K Number
K152590
Device Name
ACCU NEWS Drug Screening Test Card/Urine Cup
Manufacturer
Date Cleared
2016-04-15

(218 days)

Product Code
Regulation Number
862.3100
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The ACCU NEW® Drug Screening Test Card Urine Cup are immunochromatographic assays for the qualitative determination of the drugs/drug metabolites in human urine. The test cutoff concentrations and the tests are calibrated to are as follows: | Analyte | Abbreviation | Calibrator | Cutoff (ng/ml) | |-----------------|--------------|---------------------|----------------| | Amphetamine | AMP | d-Amphetamine | 1000 | | Methamphetamine | MET | d-Methamphetamine | 1000 | | Morphine | MOP | Morphine | 300 | | Cocaine | COC | Benzoylecgonine | 300 | | Marijuana | THC | 11-Nor-9-THC-9-COOH | 50 | The ACCU NEWS® Drug Screening Test Card /Urine Cup can consist of any combination of the drug analytes listed above. For in vitro diagnostic use only. The tests are intended for both prescription and over-the-counter (OTC) use. The device provides only a preliminary result. A more specific alternative chemical must be used in order to obtain a confirmed result. Gas Chromatography/Mass Spectrometry (GC/MS) or Liquid Chromatography/Mass Spectronetry (LCMS) are the preferred confirmatory methods. Clinical consideration and professional judgement should be exercised for any drugs of abuse test results, particularly when preliminary results are positive.
Device Description
ACCU NEWS® Drug Screening Test Card/Urine Cup is based on the principle of highly specific immunochemical reactions between antigens and antibodies. The devices utilize a competitive immunoassay in which a drug-protein conjugate immobilized on a nitrocellulose membrane competes with the drug target present in human urine for limited binding sites presented in colloidal gold-labeled mouse monoclonal antibody. The presence of a color band at a test region (coated with drug-protein conjugate) indicates a negative result for that particular test. The absence of a color band at the test region indicates presumptive positive result for that particular test. A color band at the control region, which was coasted with goat anti-mouse polyclonal antibody, should always appear regardless of the presence of the drug or its metabolites. The presence of the control band during testing serves as a built-in procedural control, indicating the completion of the test and validity of the operation. There are two formats of the test device, and both of them operate on the same basic principle. ACCU NEWS® Drug Screening Test Card device consists of individual test strips encased in a protective plastic case, and the device can detect up to 5 drugs/drug metabolites simultaneously. The ACCU NEWS® Drugs of Abuse Screening Urine Cup consists of the assembled test card integrated into a sample collection cup. Both formats are single-use, in vitro diagnostic devices. Test results interpretation: Negative: Two pink lines appear, one in the control region and the other in the test region. Regardless of the color intensity, any line formed in the test region, even if it is faint, the result is considered negative. Positive: Only one pink line appears in the control region, and no line appears in the test region. Invalid: If no line appears in the control region, the test result is invalid regardless of the absence or presence of the test line.
More Information

Not Found

No
The device description and performance studies focus on immunochemical reactions and visual interpretation of color bands, with no mention of AI or ML.

No
The device is described as an "in vitro diagnostic device" for the qualitative determination of drugs/drug metabolites in human urine, providing only a "preliminary result." It is not intended for treatment or prevention of disease.

Yes

The "Intended Use / Indications for Use" section explicitly states, "For in vitro diagnostic use only." This phrase is used to describe medical devices that are used to perform tests on samples (like urine) taken from the human body to diagnose diseases or conditions. The device determines the presence of drugs/drug metabolites in human urine, which is a diagnostic purpose.

No

The device is described as a physical test card/urine cup that utilizes immunochemical reactions on a nitrocellulose membrane to detect drugs in urine. It is an in vitro diagnostic device with physical components.

Yes, this device is an IVD (In Vitro Diagnostic).

Here's why:

  • Explicit Statement: The "Intended Use / Indications for Use" section clearly states: "For in vitro diagnostic use only."
  • Nature of the Test: The device performs a qualitative determination of drugs/drug metabolites in human urine, which is a biological sample tested in vitro (outside the body).
  • Device Description: The description details an immunochromatographic assay, a common method used in IVD tests.
  • Intended User/Care Setting: It is intended for both prescription and over-the-counter (OTC) use, indicating it's designed for diagnostic purposes, potentially by healthcare professionals or lay users.
  • Performance Studies: The document describes clinical performance studies using human urine samples to evaluate the device's performance against a reference method (GC/MS), which is standard practice for validating IVD devices.
  • Predicate Device: A predicate device (K061718) is listed, which is also an IVD drug screening test.

All these points strongly indicate that the ACCU NEW® Drug Screening Test Card Urine Cup is an In Vitro Diagnostic device.

N/A

Intended Use / Indications for Use

The ACCU NEW® Drug Screening Test Card Urine Cup are immunochromatographic assays for the qualitative determination of the drugs/drug metabolites in human urine. The test cutoff concentrations and the tests are calibrated to are as follows:

AnalyteAbbreviationCalibratorCutoff (ng/ml)
AmphetamineAMPd-Amphetamine1000
MethamphetamineMETd-Methamphetamine1000
MorphineMOPMorphine300
CocaineCOCBenzoylecgonine300
MarijuanaTHC11-Nor-9-THC-9-COOH50

The ACCU NEWS® Drug Screening Test Card /Urine Cup can consist of any combination of the drug analytes listed above.

For in vitro diagnostic use only. The tests are intended for both prescription and over-the-counter (OTC) use.

The device provides only a preliminary result. A more specific alternative chemical must be used in order to obtain a confirmed result. Gas Chromatography/Mass Spectrometry (GC/MS) or Liquid Chromatography/Mass Spectronetry (LCMS) are the preferred confirmatory methods. Clinical consideration and professional judgement should be exercised for any drugs of abuse test results, particularly when preliminary results are positive.

Product codes (comma separated list FDA assigned to the subject device)

DKZ, DJC, DJG, DIO, LDJ

Device Description

ACCU NEWS® Drug Screening Test Card/Urine Cup is based on the principle of highly specific immunochemical reactions between antigens and antibodies. The devices utilize a competitive immunoassay in which a drug-protein conjugate immobilized on a nitrocellulose membrane competes with the drug target present in human urine for limited binding sites presented in colloidal gold-labeled mouse monoclonal antibody. The presence of a color band at a test region (coated with drug-protein conjugate) indicates a negative result for that particular test. The absence of a color band at the test region indicates presumptive positive result for that particular test.

A color band at the control region, which was coasted with goat anti-mouse polyclonal antibody, should always appear regardless of the presence of the drug or its metabolites. The presence of the control band during testing serves as a built-in procedural control, indicating the completion of the test and validity of the operation.

There are two formats of the test device, and both of them operate on the same basic principle. ACCU NEWS® Drug Screening Test Card device consists of individual test strips encased in a protective plastic case, and the device can detect up to 5 drugs/drug metabolites simultaneously. The ACCU NEWS® Drugs of Abuse Screening Urine Cup consists of the assembled test card integrated into a sample collection cup. Both formats are single-use, in vitro diagnostic devices.

Test results interpretation:

Negative: Two pink lines appear, one in the control region and the other in the test region. Regardless of the color intensity, any line formed in the test region, even if it is faint, the result is considered negative.

Positive: Only one pink line appears in the control region, and no line appears in the test region.

Invalid: If no line appears in the control region, the test result is invalid regardless of the absence or presence of the test line.

Mentions image processing

Not Found

Mentions AI, DNN, or ML

Not Found

Input Imaging Modality

Not Found

Anatomical Site

human urine

Indicated Patient Age Range

Not Found

Intended User / Care Setting

The tests are intended for both prescription and over-the-counter (OTC) use.

Description of the training set, sample size, data source, and annotation protocol

Not Found

Description of the test set, sample size, data source, and annotation protocol

Not Found

Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)

Read Time Window Study:
To determine the optimal time to interpret the test results, 10 devices were tested with urine controls at negative, -50%, -25%, +25%, +50%, and +200% of cutoff concentrations.
Results: The device can be read between 3 and 8 minutes with accuracy at 95% or greater.

Precision/Sensitivity Study:
Study Type: Precision/Sensitivity study.
Sample Size: Three operators, three lots of testing devices, 6 urine samples spiked with different drug concentrations, conducted over six days.
Data Source: Urine samples spiked with different drug concentrations, confirmed with GC/MS analysis.
Annotation Protocol: Urine samples were blind-labeled and randomly distributed to operators.
Key Results:
Test Card results for AMP, MET, MOP, COC, THC at various concentrations showed expected positive/negative results relative to cutoff. For example, for AMP (cutoff: 1000 ng/ml), 30-/0+ for Neg, -50% cutoff, -25% cutoff; 6-/24+ for cutoff; 0-/30+ for +25% cutoff, +50% cutoff.
Urine Cup results for AMP, MET, MOP, COC, THC also showed expected positive/negative results relative to cutoff concentrations. For example, for AMP (cutoff: 1000 ng/ml), 30-/0+ for Neg, -50% cutoff, -25% cutoff; 16-/14+ for cutoff; 0-/30+ for +25% cutoff, +50% cutoff.

Interference Study (Chemicals):
Study Type: Interference study with common substances.
Sample Size: Three testing devices from three different lots for each spiked urine control.
Data Source: Positive urine control (+50% cutoff) and negative urine control (-50% cutoff) spiked with individual compounds at 100,000 ng/ml.
Key Results: The device was not interfered by the substances listed in Table 3.

Interference Study (pH):
Study Type: Interference study with different pH values.
Sample Size: Three testing devices from three different lots.
Data Source: Positive (+50% cutoff) and negative (-50% cutoff) urine controls with pH adjusted to 3.0, 4.0, 5.0, 6.0, 7.0, 8.0, and 9.0.
Key Results: pH values ranging from 3.0 to 9.0 in urine do not interfere with the performance.

Interference Study (Specific Gravity):
Study Type: Interference study with different specific gravity values.
Sample Size: Three testing devices from three different lots.
Data Source: Positive (+50% cutoff) and negative (-50% cutoff) urine controls with specific gravity levels of 1.001, 1.020, 1.030, and 1.040.
Key Results: The testing devices functioned properly with no interference in the specific gravity value range of 1.001 to 1.040.

Specificity (Cross-reactivity) Study:
Study Type: Specificity and cross-reactivity study.
Sample Size: Three testing devices from three different lots for each serially diluted urine sample.
Data Source: Structurally related compounds spiked into drug-free negative urine.
Key Results: Lowest concentration producing a positive test result for various structurally similar compounds and their cross-reactivity percentages were determined for both test card and urine cup formats (Table 4).

Method Comparison Study:
Study Type: Method comparison study.
Sample Size: 340 clinical urine samples.
Data Source: Clinical urine samples, with drug concentrations determined by GC/MS.
Annotation Protocol: Urine samples were blind-labeled for testing.
Key Results:
Test Card results (Table 5):
AMP: 98.0% agreement for negative and positive, 98.0% overall.
MET: 98.0% agreement for negative, 96% for positive, 97.0% overall.
MOP: 96.0% agreement for negative, 100% for positive, 98.0% overall.
COC: 98.0% agreement for negative, 96.0% for positive, 97.0% overall.
THC: 100% agreement for negative, 96.0% for positive, 98.0% overall.
Discordant results for Test Card shown in Table 6.
Urine Cup results (Table 7):
AMP: 98.0% agreement for negative and positive, 98.0% overall.
MET: 98.0% agreement for negative, 96.0% for positive, 97.0% overall.
MOP: 96.0% agreement for negative, 100% for positive, 98.0% overall.
COC: 100% agreement for negative, 96.0% for positive, 98.0% overall.
THC: 100% agreement for negative, 96.0% for positive, 98.0% overall.
Discordant results for Urine Cup shown in Table 8.

OTC Lay-User Study:
Study Type: Lay-user study.
Sample Size: 300 lay persons (175 males, 125 females) aged 18 to 47.
Data Source: Blind-labeled urine samples spiked to negative, -50% cutoff, -25% cutoff, +25% cutoff, +50% cutoff, and +100% cutoff concentrations, verified by GC/MS.
Annotation Protocol: Lay-user results compared to GC/MS results.
Key Results:
Test Card (Table 9): 100% agreement with GC/MS for AMP, MET, MOP, COC, and THC (at +100%).
Urine Cup (Table 10): 100% agreement with GC/MS for AMP, MET, MOP, COC, and 99.7% for THC.
Data showed above 95% agreement between lay-user results and GC/MS results. Lay-users found product instructions easy to understand and device easy to use.

Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)

Overall % Agreement with GC/MS (Method Comparison Study):
Test Card:
AMP: 98.0%
MET: 97.0%
MOP: 98.0%
COC: 97.0%
THC: 98.0%
Urine Cup:
AMP: 98.0%
MET: 97.0%
MOP: 98.0%
COC: 98.0%
THC: 98.0%

Agreement with GC/MS for Lay-User Study:
Test Card:
AMP: 100%
MET: 100%
MOP: 100%
COC: 100%
THC: 100%
Urine Cup:
AMP: 100%
MET: 100%
MOP: 100%
COC: 100%
THC: 99.7%

Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.

K061718

Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.

Not Found

Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).

Not Found

§ 862.3100 Amphetamine test system.

(a)
Identification. An amphetamine test system is a device intended to measure amphetamine, a central nervous system stimulating drug, in plasma and urine. Measurements obtained by this device are used in the diagnosis and treatment of amphetamine use or overdose and in monitoring levels of amphetamine to ensure appropriate therapy.(b)
Classification. Class II (special controls). An amphetamine test system is not exempt if it is intended for any use other than employment or insurance testing or is intended for Federal drug testing programs. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 862.9, provided the test system is intended for employment and insurance testing and includes a statement in the labeling that the device is intended solely for use in employment and insurance testing, and does not include devices intended for Federal drug testing programs (e.g., programs run by the Substance Abuse and Mental Health Services Administration (SAMHSA), the Department of Transportation (DOT), and the U.S. military).

0

Image /page/0/Picture/1 description: The image shows the seal of the Department of Health & Human Services (HHS) of the United States. The seal is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the seal, there is a stylized image of three faces in profile, representing the department's mission to protect the health of all Americans and provide essential human services.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

April 15, 2016

CORETESTS, INC. ERIC SUN REGULATORY AFFAIRS SCIENTIST 6190 YARROW DRIVE CARLSBAD, CA 92011

Re: K152590

Trade/Device Name: ACCU NEWS Drug Test Card/Urine Cup Regulation Number: 21 CFR 862.3100 Regulation Name: Amphetamine Test System Regulatory Class: II Product Code: DKZ, DJC, DJG, DIO, and LDJ Dated: March 11, 2016 Received: March 16, 2016

Dear Eric Sun:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Parts 801 and 809); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the

1

electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely vours.

Courtney H. Lias -S

Courtney H. Lias, Ph.D. Director Division of Chemistry and Toxicology Devices Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health

Enclosure

2

DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration

Indications for Use

Form Approved: OMB No. 0910-0120 Expiration Date: January 31, 2017 See PRA Statement below

510(k) Number (if known) K152590

Device Name ACCU NEW® Drug Screening Test Card ACCU NEW® Drug Screening Urine Cup

Indications for Use (Describe)

The ACCU NEW® Drug Screening Test Card Urine Cup are immunochromatographic assays for the qualitative determination of the drugs/drug metabolites in human urine. The test cutoff concentrations and the tests are calibrated to are as follows:

AnalyteAbbreviationCalibratorCutoff (ng/ml)
AmphetamineAMPd-Amphetamine1000
MethamphetamineMETd-Methamphetamine1000
MorphineMOPMorphine300
CocaineCOCBenzoylecgonine300
MarijuanaTHC11-Nor-9-THC-9-COOH50

The ACCU NEWS® Drug Screening Test Card /Urine Cup can consist of any combination of the drug analytes listed above.

For in vitro diagnostic use only. The tests are intended for both prescription and over-the-counter (OTC) use.

The device provides only a preliminary result. A more specific alternative chemical must be used in order to obtain a confirmed result. Gas Chromatography/Mass Spectrometry (GC/MS) or Liquid Chromatography/Mass Spectronetry (LCMS) are the preferred confirmatory methods. Clinical consideration and professional judgement should be exercised for any drugs of abuse test results, particularly when preliminary results are positive.

Type of Use (Select one or both, as applicable)

Prescription Use (Part 21 CFR 801 Subpart D)

Over-The-Counter Use (21 CFR 801 Subpart C)

CONTINUE ON A SEPARATE PAGE IF NEEDED.

This section applies only to requirements of the Paperwork Reduction Act of 1995.

DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.

The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:

Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov

"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."

FORM FDA 3881 (8/14)

POC Publishing Services (100) 443-6740 17

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510k Summary

A. Submitter Information

Coretests Inc.

6190 Yarrow Drive, Carlsbad, CA 92011, USA.

Phone Number: 858-333-1122

Contact Person: Eric Sun (Regulatory Affairs Scientist)

Summary Prepared on March 11, 2016

B. Trade Name, common name, classification name

Trade Name: ACCU NEWS® Drug Screening Test Card/Urine Cup containing one to five of the following drug of abuse test(s) in each device: Amphetamine, Methamphetamine, Morphine, Cocaine, & Marijuana

Common Name: Oualitative Lateral Flow Immunoassay

Classification: Class II

Panel: Toxicology 91

| Drug of Abuse | Product
Code | Regulation Section |
|-----------------|-----------------|-----------------------------------------------------------------|
| Amphetamine | DKZ | 21 CFR 862.3100, Amphetamine Test System |
| Methamphetamine | DJC | 21 CFR 862.3610, Methamphetamine Test System |
| Morphine | DJG | 21 CFR 862.3640, Morphine Test System |
| Cocaine | DIO | 21 CFR 862.3250, Cocaine and Cocaine Metabolites
Test System |
| Marijuana | LDJ | 21 CFR 862.3870, Cannabinoids Test System |

C. Predicate Device

K061718 Innovacon® Spectrum II Test Card/Test Card with Integrated Cups

D. Device Description

ACCU NEWS® Drug Screening Test Card/Urine Cup is based on the principle of highly specific immunochemical reactions between antigens and antibodies. The devices utilize a competitive immunoassay in which a drug-protein conjugate immobilized on a nitrocellulose membrane competes with the drug target present in human urine for limited binding sites presented in colloidal gold-labeled mouse monoclonal antibody. The presence of a color band at a test region (coated with drug-protein conjugate) indicates a

4

negative result for that particular test. The absence of a color band at the test region indicates presumptive positive result for that particular test.

A color band at the control region, which was coasted with goat anti-mouse polyclonal antibody, should always appear regardless of the presence of the drug or its metabolites. The presence of the control band during testing serves as a built-in procedural control, indicating the completion of the test and validity of the operation.

There are two formats of the test device, and both of them operate on the same basic principle. ACCU NEWS® Drug Screening Test Card device consists of individual test strips encased in a protective plastic case, and the device can detect up to 5 drugs/drug metabolites simultaneously. The ACCU NEWS® Drugs of Abuse Screening Urine Cup consists of the assembled test card integrated into a sample collection cup. Both formats are single-use, in vitro diagnostic devices.

Test results interpretation:

Negative: Two pink lines appear, one in the control region and the other in the test region. Regardless of the color intensity, any line formed in the test region, even if it is faint, the result is considered negative.

Positive: Only one pink line appears in the control region, and no line appears in the test region.

Invalid: If no line appears in the control region, the test result is invalid regardless of the absence or presence of the test line.

E. Intended Use

Coretests Inc.'s ACCU NEWS® Drug Screening Test Card/Urine Cup is a qualitative lateral flow for screening drugs/drug metabolites in human urine to aid detection of drugs of abuse. The test devices are for both prescription and over-the-counter (OTC) use.

F. Summary of the technological characteristics of your device compared to the predicate device

Similarities and Differences
FeatureCandidate DevicesPredicate Devices
(K061718)

5

| Intended Use | For detection of drugs/drug
metabolites in human urine to
screen for drugs of abuse. | Same |
|--------------------------------|---------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------|
| Specimen | Human urine | Same |
| Results | Qualitative | Same |
| Methodology | Competitive Lateral Flow
Immunoassay | Same |
| Intended Users | Prescription and over-the-
counter (OTC) users | Prescription users |
| Analytes and
Cutoff (ng/ml) | Amphetamine – 1000
Cocaine - 300
Methamphetamine – 1000
Morphine - 300
Marijuana - 50 | Amphetamine – 1000/300
Cocaine - 300/150
Methamphetamine – 1000/500
Morphine - 2000/300
Marijuana - 50 |
| Storage
Temperature | 2-30°C (36-86°F) | Same |
| Formats | Test Card and Urine Cup | Same |

G. Non-clinical performance data

a. Read Time Window

To determine the optimal time to interpret the test results of ACCU NEWS® Drug Screening Test Card/Urine Cup, 10 devices were tested with urine controls at the following concentration: negative, -50%, -25%, +25%, +50% and +200% of cutoff. Based on the test results, ACCU NEWS® Drug Screening Test Card/Urine Cup can be read between 3 and 8 minutes with accuracy at 95% or greater.

b. Precision/Sensitivity

The precision study was conducted by three (3) operator with three (3) lots of testing devices using a total of 6 urine samples spiked with different drug concentrations: negative, -50%, -25%, cutoff, +25%, and +50% of cutoff concentrations. The drug concentrations in the urine samples were confirmed with GC/MS analysis. These urine samples were blind-labeled and randomly distributed by the project coordinator to the three operators. The study was conducted in six days. The results were summarized below:

Table 1: Summary of Precision/Sensitivity Data - Test Card AMP (cutoff: 1000 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|--------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 6-/24+ | 0-/30+ | 0-/30+ |

6

MET (cutoff: 1000 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|---------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 10-/20+ | 0-/30+ | 0-/30+ |

MOP (cutoff: 300 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|--------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 7-/23+ | 0-/30+ | 0-/30+ |

COC (cutoff: 300 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|--------|----------------|----------------|
| 30-/0+ | 30-/0+ | 29-/1+ | 21-/9+ | 1-/29+ | 0-/30+ |

THC (cutoff: 50 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|--------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 24-/6+ | 2-/28+ | 0-/30+ |

Table 2: Summary of Precision/Sensitivity Data – Urine Cup AMP (cutoff: 1000 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|---------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 16-/14+ | 0-/30+ | 0-/30+ |

MET (cutoff: 1000 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|---------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 14-/16+ | 1-/29+ | 0-/30+ |

MOP (cutoff: 300 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|---------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 17-/13+ | 2-/28+ | 0-/30+ |

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COC (cutoff: 300 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|---------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 19-/11+ | 2-/28+ | 0-/30+ |

THC (cutoff: 50 ng/ml)

| Neg. | -50%
cutoff | -25%
cutoff | cutoff | +25%
cutoff | +50%
cutoff |
|--------|----------------|----------------|--------|----------------|----------------|
| 30-/0+ | 30-/0+ | 30-/0+ | 23-/7+ | 0-/30+ | 0-/30+ |

c. Interference

1. Chemicals

To determine if common substances possibly found in human urine in physiological or pathological conditions would react and interfere with ACCU NEWS® Drug Screening Test Card/Urine Cup, positive urine control (+50% cutoff) and negative urine control (-50% cutoff) were spiked with individual compounds at 100,000 ng/ml. Each spiked urine control was tested with three (3) testing devices from three (3) different lots. Results showed that the ACCU NEWS® Drug Screening Test Card/Urine Cup was not interfered by the substances listed below.

Table 3. List of Compounds showing no interference
Acetylsalicylic AcidDextromethorphanMeprobamatePrednisone
AminopyrineDiclofenacNalidixic acidD,L-Propanolol
AmoxicillinDiflunisalNaloxoneD-Pseudoephedrine
AmpicillinDigoxinNaltrexoneQuinidine
ApomorphineDiphenhydramineMethoxyphenamineQuinine
AspartameEcgonine methyl esterNaproxenRanitidine
AtropineL-ψ-EphedrineNiacinamideSalicylic acid
Benzilic acidEthyl-p-aminobenzoateNifedipineSerotonin
Benzoic acidErythromycinNorethindroneSulfamethazine
Bilirubinβ-EstradiolD-NorpropoxypheneTetrahydrozoline
CaffeineFenoprofenNoscapineThiamine
Chloral hydrateFurosemideD,L-OctopamineThioridazine
ChloramphenicolGentisic acidOxalic acidD,L-Tyrosine
ChlorothiazideHemoglobinOxolinic acidTriamterene
D,L-ChlolrpheniramineHydralazineOxymetazolineTrifluoperazine
ChlorpromazineHydrochlorothiazidePapaverineTrimethoprim
ChloroquineHydrocortisonePenicillin-GTyramine
Cholesterol3-HydroxytyraminePerphenazineD,L-Tryptophan
ClonidineD,L-IsoproterenolPhenacetinUric acid
CortisoneIsoxsuprinePhenelzineVerapamil
L-CotinineKetoprofenL-PhenylephrineZomepirac
CreatinineLabetalolβ-Phenylethylamine
DeoxycortisteroneLoperamidePhenylpropanolamine

Table 3: List of Compounds showing no interference

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2. pH

To determine if different pH values in urine would affect ACCU NEWS® Drug Screening Test Card/Urine Cup, three (3) testing devices from three (3) different lots were tested with positive (+50% cutoff) and negative (-50% cutoff) urine controls with pH adjusted to the following values: 3.0. 4.0, 5.0. 6.0, 7.0. 8.0, and 9.0. Experimental results indicated that pH values ranging from 3.0 to 9.0 in urine do not interfere with the performance of the testing device.

3. Specific Gravity

To determine if different specific gravity values in urine can affect ACCU NEWS® Drug Screening Test Card/Urine Cup, positive (+50% cutoff) and negative (-50% cutoff) urine controls with the following specific gravity levels, 1.001, 1.020. 1.030 and 1.040, were tested. Three (3) testing devices from three (3) different lots were tested with each urine control. Result showed that the testing devices functioned properly with no interference in the specific gravity value range of 1.001 to 1.040.

d. Specificity

ACCU NEWS® Drug Screening Test Card/Urine Cup were tested for specificity and cross-reactivity by testing with structurally related compounds spiked into drug-free negative urine. Three (3) testing devices from three (3) different lots were tested for each serially diluted urine sample, and the lowest concentration producing a positive test result was determined for each structurally related compounds in the following table produced positive results when tested at or above the concentrations listed below; the results were the same for both test card and urine cup formats:

Drug TestCompoundConc. (ng/ml)% Cross-reactivity
AMPd-Amphetamine1,000100
d,l-Amphetamine3,00033.3
l-Amphetamine50,0002
d-Methamphetamine>100,000100,000
cutoff)% Agreement with
GC/MSOverall %
Agreement
with
GC/MS
-----------------------------------------------------------------------------------------------
AMP+01
-409
MET+01
-409
MOP+02
-408
COC+01
-409
THC+00
-4010

Table 5: Summary of Method Comparison Data – Test Card

Table 6: Summary of Discordant Results – Test Card

| Sample | Drug Test | Results
Recorded | GC/MS Value
(ng/mL) |
|--------|-----------|---------------------|------------------------|
| 844591 | AMP 1000 | Positive | 952 |
| 545390 | AMP 1000 | Negative | 1030 |
| 960940 | MET 1000 | Positive | 982 |
| 860829 | MET 1000 | Negative | 1054 |
| 610670 | MET 1000 | Negative | 1060 |
| 572595 | MOP 300 | Positive | 284 |
| 898906 | MOP 300 | Positive | 286 |

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699527COC 300Positive285
710595COC 300Negative322
491069COC 300Negative330
494372THC 50Negative54.3
801073THC 50Negative55.0

Table 7: Summary of Method Comparison Data – Urine Cup

| | | No Drug
Present | Near Cutoff
Negative
(between -
50% cutoff
and cutoff | Near Cutoff
Positive
(between
cutoff and
+50% cutoff) | High
Positive
(> +50%
cutoff) | % Agreement with
GC/MS | | Overall %
Agreement
with
GC/MS |
|-----|---|--------------------|-------------------------------------------------------------------|-------------------------------------------------------------------|----------------------------------------|---------------------------|----------|-----------------------------------------|
| | | | | | | Negative | Positive | |
| AMP | + | 0 | 1 | 9 | 40 | 98.0% | 98.0% | 98.0% |
| | - | 40 | 9 | 1 | 0 | | | |
| MET | + | 0 | 1 | 8 | 40 | 98.0% | 96.0% | 97.0% |
| | - | 40 | 9 | 2 | 0 | | | |
| MOP | + | 0 | 2 | 10 | 40 | 96.0% | 100% | 98.0% |
| | - | 40 | 8 | 0 | 0 | | | |
| COC | + | 0 | 0 | 8 | 40 | 100% | 96.0% | 98.0% |
| | - | 40 | 10 | 2 | 0 | | | |
| THC | + | 0 | 0 | 8 | 40 | 100% | 96.0% | 98.0% |
| | - | 40 | 10 | 2 | 0 | | | |

Table 8: Summary of Discordant Results – Urine Cup

| Sample | Drug Test | Results
Recorded | GC/MS Value
(ng/mL) |
|--------|-----------|---------------------|------------------------|
| 844591 | AMP 1000 | Positive | 952 |
| 545390 | AMP 1000 | Negative | 1030 |
| 960940 | MET 1000 | Positive | 982 |
| 860829 | MET 1000 | Negative | 1054 |
| 610670 | MET 1000 | Negative | 1060 |
| 572595 | MOP 300 | Positive | 284 |
| 898906 | MOP 300 | Positive | 286 |
| 710595 | COC 300 | Negative | 322 |
| 491069 | COC 300 | Negative | 330 |
| 494372 | THC 50 | Negative | 54.3 |
| 801073 | THC 50 | Negative | 55.0 |

H. Clinical performance data

  • a. Clinical Sensitivity: Not Applicable
  • b. Clinical Specificity: Not Applicable

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c. Other Clinical Supportive Data:

OTC Lay-User Study

A lay-user study was conducted at 3 sites with 300 lay persons. A total of 175 males and 125 females from ages of 18 to 47 with a variety of educational background participated in the study. The blind-labeled urine samples were spiked to the following concentrations: negative urine, -50% cutoff, -25% cutoff, +25% cutoff, +50% cutoff, and +100% cutoff. All the samples were verified by GC/MS, and the results of lay-user were compared to those of GC/MS.

| Table 9: Summary of Lay-User Result Data – Test Card | | | | | | | Agreement
with GC/MS | |
|------------------------------------------------------|---------|----------|------|------|------|------|-------------------------|-------|
| Drug | Results | Negative | -50% | -25% | +25% | +50% | | +100% |
| AMP | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| MET | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| MOP | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| COC | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| THC | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |

Table 0: Summary of Lay User Racult Dota - Tact Card

Table 10: Summary of Lay-User Result Data - Urine Cup

| Drug | Results | Drug Concentration | | | | | | Agreement
with GC/MS |
|------|---------|--------------------|------|------|------|------|-------|-------------------------|
| | | Negative | -50% | -25% | +25% | +50% | +100% | |
| AMP | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| MET | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| MOP | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| COC | + | 0 | 0 | 0 | 20 | 40 | 20 | 100% |
| | - | 180 | 20 | 20 | 0 | 0 | 0 | |
| THC | + | 0 | 0 | 0 | 19 | 40 | 20 | 99.7% |
| | - | 180 | 20 | 20 | 1 | 0 | 0 | |

For both ACCU NEWS® Drug Screening Test Card/Urine Cup, Data showed above 95% agreement between lay-user results and GC/MS results. This demonstrated that the devices were easy enough to be used by untrained lay-users. In addition, each subject was given questionnaires in English to assess the readability of the labeling.

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The results showed that the lay-users found the product instruction to be easy to understand and the device to be easy to use.

I. Conclusion

The performance characteristics studies performed demonstrated substantial equivalency between ACCU NEWS® Drug Screening Test Card/Urine Cup and Innovacon® Spectrum II Test Card/Test Card with Integrated Cups.