(124 days)
Not Found
No
The device description details a homogeneous enzyme immunoassay and the associated reagents and calibrators. There is no mention of AI or ML in the intended use, device description, or performance studies. The technology described is a standard immunoassay method.
No.
The device is an in vitro diagnostic (IVD) product used for the semi-quantitative or qualitative determination of amphetamines in human urine. It is used in the diagnosis and treatment of amphetamines use or overdose, but it is not a therapeutic device itself.
Yes
The "Intended Use / Indications for Use" section explicitly states, "Measurements obtained with the VITROS AMPH method are used in the diagnosis and treatment of amphetamines use or overdose."
No
The device description clearly outlines physical reagents (VITROS Chemistry Products AMPH Reagent, Calibrator Kit 26, FS Calibrator 1, FS Diluent Pack 4, DAT Performance Verifiers) and the VITROS 5,1 FS Chemistry System, which is a clinical chemistry instrument. This indicates a hardware-based system with associated reagents, not a software-only device.
Based on the provided text, the device is an IVD (In Vitro Diagnostic).
Here's why:
- Explicit Statement: The "Intended Use / Indications for Use" section explicitly states "For in vitro diagnostic use only." multiple times for the different components of the system (Reagent, Calibrator Kit, Calibrator 1, Performance Verifiers).
- Purpose: The device is used for the "semi-quantitative or qualitative determination of amphetamines (AMPH) in human urine." This is a test performed on a biological sample (urine) outside of the body to provide information for diagnosis and treatment.
- Method: The description details a "homogeneous enzyme immunoassay," which is a common in vitro diagnostic technique.
- Components: The system includes reagents, calibrators, and controls, which are typical components of IVD assays.
- Intended User: The intended user is "professional laboratory personnel," indicating use in a laboratory setting for diagnostic purposes.
Therefore, the device clearly fits the definition of an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
For in vitro diagnostic use only. VITROS Chemistry Products AMPH Reagent is used on VITROS 5,1 FS Chemistry Systems for the semi- quantitative or qualitative determination of amphetamines (AMPH) in human urine using a cutoff of either 500 or 1000 ng/mL. Measurements obtained with the VITROS AMPH method are used in the diagnosis and treatment of amphetamines use or overdose. The VITROS Chemistry Products AMPH assay is intended for use by professional laboratory personnel. It provides only a preliminary test result. A more specific alternative chemical method must be used to confirm a result obtained with this assay. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method Clinical consideration and professional judgment should be applied to any drug-of-abuse test result, particularly when evaluating a preliminary positive result.
For in vitro diagnostic use only. VITROS Chemistry Products Calibrator Kit 26 is used to calibrate VITROS 5,1 FS Chemistry Systems for the qualitative or semi-quantitative measurement of drugs of abuse.
For in vitro diagnostic use only. VITROS Chemistry Products FS Calibrator 1 is used in conjunction with VITROS Chemistry Products Calibrator Kits to calibrate VITROS 5,1 FS Chemistry Systems.
For in vitro diagnostic use only. VITROS Chemistry Products DAT Performance Verifiers are assayed controls used to monitor performance of urine drugs of abuse screening assays on VITROS 5.1 FS Chemistry Systems.
Product codes
DKZ, DLJ, DIF
Device Description
The VITROS AMPH assay is a homogeneous enzyme immunoassay that is performed using the VITROS Chemistry Products AMPH Reagent with the VITROS Chemistry Products Calibrator Kit 26, VITROS Chemistry Products FS Calibrator 1, and VITROS Chemistry Products FS Diluent Pack 4 (DAT Diluent / DAT Diluent 2) on VITROS 5,1 FS Chemistry Systems.
The VITROS AMPH Reagent is a dual chambered package containing ready-to-use liquid reagents that are used to detect amphetamines in urine. Sample, calibrators, and controls are automatically treated with surfactant (DAT Diluent 2) prior to addition of reagents. Treated sample is added to Reagent 1 containing antibodies reactive to d-amphetamine and d-methamphetamine, glucose-6-phosphate and nicotinamide adenine dinucleotide (NAD*), followed by Reagent 2 containing damphetamine and d-methamphetamine, both labeled with the enzyme glucose-6phosphate dehydrogenase (G6P-DH). The assay is based on competition between amphetamines in the treated urine sample and the d-amphetamine and dmethamphetamine labeled with the enzyme glucose-6-phosphate dehydrogenase (G6P-DH) for antibody binding sites. Enzyme activity decreases upon binding to the antibody, therefore the concentration of amphetamines in the urine sample is directly proportional to measured enzyme activity. Active enzyme converts oxidized nicotinamide adenine dinucleotide (NAD*) to NADH, resulting in an absorbance change that is measured spectrophotometrically at 340 nm.
The VITROS Chemistry Products Calibrator Kit 26 is prepared from human urine to which drugs of abuse, metabolites of drugs of abuse, organic salt, surfactants, and preservative have been added. VITROS Chemistry Products FS Calibrator 1 is prepared from sodium chloride and processed water. These standards are used to calibrate VITROS 5,1 FS Chemistry Systems for the qualitative and semiquantitative measurement of amphetamines (AMPH).
The VITROS Chemistry Products DAT Performance Verifiers I, II, III, IV, and V are quality control materials prepared from a human urine pool to which analytes, surfactant, and preservative have been added. These are assayed controls used to monitor performance of VITROS AMPH assay on VITROS 5,1 FS Chemistry Systems.
The VITROS Chemistry Products FS Diluent Pack 4 (DAT Diluent / DAT Diluent 2) is a common reagent that is used by multiple assays on the VITROS 5,1 FS Chemistry System. This is a dual chambered package containing two ready-to-use liquid diluents. DAT Diluent is prepared from human urine to which organic salt, surfactants, and preservative have been added. DAT Diluent 2 is prepared from processed water to which surfactant and preservative have been added.
The VITROS 5,1 FS Chemistry System is a clinical chemistry - instrument that provides automated use of the VITROS Chemistry Products MicroTip® and MicroSlides® range of products. The VITROS 5,1 FS System was cleared for market by 510(k) premarket notification (K031924).
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
professional laboratory personnel
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)
The performance of the VITROS AMPH assay on the VITROS 5,1 FS Chemistry System was compared to the Syva® EMIT II Plus Amphetamines assay on the SYVA 30R System. The results demonstrated good agreement between the two immunoassay methods.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
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
This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR 807.92.
The assigned 510(k) number is: _K 06 2017
- Ortho-Clinical Diagnostics, Inc. 1. Submitter 100 Indigo Creek Drive name. Rochester, New York 14626-5101 address, (585) 453-4041 contact Contact Person: Marlene Hanna
- September 25, 2006 2. Preparation Date
- Trade or Proprietary Names: 3. Device name VITROS Chemistry Products AMPH Reagent VITROS Chemistry Products Calibrator Kit 26 VITROS Chemistry Products FS Calibrator 1 VITROS Chemistry Products DAT Performance Verifiers I, II, III, IV, and V
Common Names: Amphetamine assay and controls and controls
Classification Names:
-
Amphetamine test system (21 CFR 862.3100) Class II
-
Clinical toxicology calibrators (21 CFR 862.3200) Class II
-
Clinical toxicology control material (21 CFR 862.3280) DAT Performance
Verifiers I, II ,III, IV , andV ) are assayed controls, so they meet the reserved criteria under Section 510(1) of the Food, Drug, and Cosmetic Act.
Continued on next page
1
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- Predicate The VITROS Chemistry Products AMPH assay is substantially equivalent to the Devices Syva® EMIT II Plus Amphetamines assay.
The VITROS Chemistry Products DAT Performance Verifiers are substantially equivalent to the Bio-Rad Liquicheck™ UrineToxicology Controls.
- Predicate The VITROS Chemistry Products AMPH assay is substantially equivalent to the Devices Syva® EMIT II Plus Amphetamines assay.
-
The VITROS AMPH assay is a homogeneous enzyme immunoassay that is 5. Device description performed using the VITROS Chemistry Products AMPH Reagent with the VITROS Chemistry Products Calibrator Kit 26, VITROS Chemistry Products FS Calibrator 1, and VITROS Chemistry Products FS Diluent Pack 4 (DAT Diluent / DAT Diluent 2) on VITROS 5,1 FS Chemistry Systems.
The VITROS AMPH Reagent is a dual chambered package containing ready-to-use liquid reagents that are used to detect amphetamines in urine. Sample, calibrators, and controls are automatically treated with surfactant (DAT Diluent 2) prior to addition of reagents. Treated sample is added to Reagent 1 containing antibodies reactive to d-amphetamine and d-methamphetamine, glucose-6-phosphate and nicotinamide adenine dinucleotide (NAD*), followed by Reagent 2 containing damphetamine and d-methamphetamine, both labeled with the enzyme glucose-6phosphate dehydrogenase (G6P-DH). The assay is based on competition between amphetamines in the treated urine sample and the d-amphetamine and dmethamphetamine labeled with the enzyme glucose-6-phosphate dehydrogenase (G6P-DH) for antibody binding sites. Enzyme activity decreases upon binding to the antibody, therefore the concentration of amphetamines in the urine sample is directly proportional to measured enzyme activity. Active enzyme converts oxidized nicotinamide adenine dinucleotide (NAD*) to NADH, resulting in an absorbance change that is measured spectrophotometrically at 340 nm.
The VITROS Chemistry Products Calibrator Kit 26 is prepared from human urine to which drugs of abuse, metabolites of drugs of abuse, organic salt, surfactants, and preservative have been added. VITROS Chemistry Products FS Calibrator 1 is prepared from sodium chloride and processed water. These standards are used to calibrate VITROS 5,1 FS Chemistry Systems for the qualitative and semiquantitative measurement of amphetamines (AMPH).
The VITROS Chemistry Products DAT Performance Verifiers I, II, III, IV, and V are quality control materials prepared from a human urine pool to which analytes, surfactant, and preservative have been added. These are assayed controls used to monitor performance of VITROS AMPH assay on VITROS 5,1 FS Chemistry Systems.
Continued on next page
2
- Device
intended uses
The VITROS Chemistry Products FS Diluent Pack 4 (DAT Diluent / DAT Diluent 2) is a common reagent that is used by multiple assays on the VITROS 5,1 FS Chemistry System. This is a dual chambered package containing two ready-to-use liquid diluents. DAT Diluent is prepared from human urine to which organic salt, surfactants, and preservative have been added. DAT Diluent 2 is prepared from processed water to which surfactant and preservative have been added.
The VITROS 5,1 FS Chemistry System is a clinical chemistry - instrument that provides automated use of the VITROS Chemistry Products MicroTip® and MicroSlides® range of products. The VITROS 5,1 FS System was cleared for market by 510(k) premarket notification (K031924).
VITROS Chemistry Products AMPH Reagent: For in vitro diagnostic use only. VITROS Chemistry Products AMPH Reagent is used on VITROS 5,1 FS Chemistry Systems for the semi-quantitative or qualitative determination of amphetamines (AMPH) in human urine using a cutoff of either 500 or 1000 ng/mL. Measurements obtained with the VITROS AMPH method are used in the diagnosis and treatment of amphetamines use or overdose.
The VITROS Chemistry Products AMPH assay is intended for use by professional laboratory personnel. It provides only a preliminary test result. A more specific alternative chemical method must be used to confirm a result obtained with this assay. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug-of-abuse test result, particularly when evaluating a preliminary positive result.
VITROS Chemistry Products Calibrator Kit 26: For in vitro diagnostic use only. VITROS Chemistry Products Calibrator Kit 26 is used to calibrate VITROS 5,1 FS Chemistry Systems for the qualitative or semi-quantitative measurement of drugs of abuse.
VITROS Chemistry Products FS Calibrator 1: For in vitro diagnostic use only. VITROS Chemistry Products FS Calibrator 1 is used in conjunction with VITROS Chemistry Products Calibrator Kits to calibrate VITROS 5,1 FS Chemistry Systems
VITROS Chemistry Products DAT Performance Verifiers I, II, III, IV, and V: For in vitro diagnostic use only. VITROS Chemistry Products DAT Performance Verifiers are assayed controls used to monitor performance of urine drugs of abuse screening assays on VITROS 5,1 FS Chemistry Systems. .
-
- Comparison The VITROS Chemistry Products AMPH assay and VITROS Chemistry Products DAT Performance Verifiers are substantially equivalent to the Syva® EMIT II Plus to predicate Amphetamines assay (K031004) and Bio-Rad Liquicheck™ Urine Toxicology devices: Controls (K022707) predicate devices which were cleared by the FDA for IVD use.
Continued on next page
- Comparison The VITROS Chemistry Products AMPH assay and VITROS Chemistry Products DAT Performance Verifiers are substantially equivalent to the Syva® EMIT II Plus to predicate Amphetamines assay (K031004) and Bio-Rad Liquicheck™ Urine Toxicology devices: Controls (K022707) predicate devices which were cleared by the FDA for IVD use.
3
The performance of the VITROS AMPH assay on the VITROS 5,1 FS Chemistry System was compared to the Syva® EMIT II Plus Amphetamines assay on the SYVA 30R System. The results demonstrated good agreement between the two immunoassay methods.
The VITROS AMPH assay and VITROS DAT Controls have the following similarities to the predicate devices: same intended use, the same cutoff values of 500 and 1000 ng/mL, are liquid, ready to use reagents, have similar performance characteristics, are used on an automated clinical chemistry analyzer and calibrated against the same drug, methamphetamine.
Similarities and differences of the assays performed using the VITROS AMPH assay and Table 1 DAT controls and the Syva EMIT II Plus Amphetamines assay and Bio-Rad Urine Toxicology controls.
| Device Similarities | ||
|---|---|---|
| Device Characteristic | Description | |
| Indications for Use | For in vitro diagnostic use only. The assays are intended for use in the qualitative | |
| and semi-quantitative analysis of amphetamines in human urine. The controls are | ||
| assayed controls used to monitor the performance of Chemistry Systems. | ||
| Test Principle | Homogeneous enzyme immunoassay | |
| Cut-Off values | 500 or 1000 ng/mL | |
| Specimen Type | Human Urine | |
| Reagent Format | Liquid ready to use | |
| Antibody source | Mouse monoclonal antibodies reactive to d-amphetamine and d-metamphetamine | |
| Calibration traceability | d-metamphetamines with confirmation by GC/MS | |
| Calibrator matrix | Human urine | |
| Control matrix | Human urine | |
| Device Differences | ||
| Device Characteristic | VITROS AMPH assay | |
| (New device) | Emit® Amphetamines assay | |
| (Predicate device) | ||
| Cut-Off values | 500 or 1000 ng/mL | 300, 500, or 1000 ng/mL |
| Calibrator levels | 6 levels | Qualitative: Two levels |
| Semi-quantitative: 300 ng/mL Cutoff | ||
| value: Four levels; 500 and 1000 ng/mL | ||
| cutoff values: Five levels | ||
| Calibrator format | Frozen Liquid ready to use | Refrigerated liquid ready to use |
| Instrumentation | To be used on VITROS 5,1 FS | |
| Chemistry Systems | Multiple automated clinical chemistry | |
| systems | ||
| Controls: Drugs | ||
| Reported | Cocaine metabolites | |
| (benzoylecgonine), | ||
| benzodiazepines (lormetazepam), | ||
| methadone, amphetamines (d- | ||
| methamphetamine), opiates | ||
| (morphine), cannabinoids (11-nor- | ||
| delta-THC-9-COOH), | ||
| phencyclidine and barbiturates | ||
| (secobarbital). | Methamphetamine, secobarbital, | |
| lormetazepam, tetrahydrocannabinol | ||
| (THC), benzoylecgonine, ethanol, lysergic | ||
| acid diethylamide (LSD), methadone, | ||
| methaqualone, morphine, (Free), | ||
| phencyclid ine, propoxyphene. | ||
| nortriptyline and addition of creatinine, | ||
| pH, specific gravity. | ||
| Controls: Number of | ||
| Levels | Five | Two |
4
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- Conclusions The data presented in the premarket notification provide a reasonable assurance that the VITROS Chemistry Products AMPH Reagent, VITROS Chemistry Products Calibrator Kit 26, VITROS Chemistry Products FS Calibrator 1, and the VITROS Chemistry Products DAT Performance Verifiers are safe and effective for the stated intended uses and are substantially equivalent to the cleared predicate devices. Equivalence to the predicates was demonstrated using a commercially available assay along with patient samples.
5
Image /page/5/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a stylized eagle with three tail feathers. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES. USA" are arranged in a circle around the eagle.
Food and Drug Administration 2098 Gaither Road Rockville MD 20850
Ms. Marlene Hanna Regulatory Affairs Manager Ortho Clinical Diagnostics Inc. 100 Indigo Creek Drive Rochester, NY 14626-5101
NOV 2 2 2006
Re: k0602077
Trade/Device Name: VITROS Chemistry Products AMPH Reagent VITROS Chemistry Products Calibrator Kit 26 VITROS Chemistry Products FS Calibrator 1 VITROS Chemistry Products DAT Performance Verifiers I, II, III, IV, and V Regulation Number: 21 CFR 862.3100 Regulation Name: Amphetamine test system Regulatory Class: Class II Product Code: DKZ, DLJ, DIF Dated: September 27, 2006 Received: September 28, 2006
Dear Ms. Hanna:
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 cnactment 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.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in Title 21, Code of Federal Regulations (CFR), Parts 800 to 895. 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
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Page 2 -
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); and good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820).
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific information about the application of labcling requirements to your device, or questions on the promotion and advertising of your device, please contact the Office of In Vitro Diagnostic Device Evaluation and Safety at (301) 594-3084. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html.
Sincerely yours.
Carol Bensonfor
Alberto Gutierrez, Ph.D. Director Division of Chemistry and Toxicology Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health
Enclosure
7
Indications for Use
Page 1 of 2
| 510(k) Number (if known): | K062077 |
|---|---|
| Device Name: | VITROS Chemistry Products AMPH Reagent |
| Indications for Use: | For in vitro diagnostic use only. VITROS Chemistry Products AMPH Reagent is used on VITROS 5,1 FS Chemistry Systems for the semi- quantitative or qualitative determination of amphetamines (AMPH) in human urine using a cutoff of either 500 or 1000 ng/mL. Measurements obtained with the VITROS AMPH method are used in the diagnosis and treatment of amphetamines use or overdose. The VITROS Chemistry Products AMPH assay is intended for use by professional laboratory personnel. It provides only a preliminary test result. A more specific alternative chemical method must be used to confirm a result obtained with this assay. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method Clinicol |
spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug-of-abuse test result, particularly when evaluating a preliminary positive result.
Prescription Use __ × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use __ (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Carol Benson
Revision Sign-Off
ision Sign-Off
Office of In Vitro Diagnostic Device Evaluation and Safety
KO 60 77 ﺎ ﻓﻲ ﺍﻟﻤﺴﺘﻮﻯ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ
8
Indications for Use
Page 2 of 2
510(k) Number (if known):
Device Name:
VITROS Chemistry Products Calibrator Kit 26 VITROS Chemistry Products FS Calibrator 1 VITROS Chemistry Products DAT Performance Verifiers I, II, III, IV, and V.
Indications for For in vitro diagnostic use only. VITROS Chemistry Products Use: Calibrator Kit 26 is used to calibrate VITROS 5,1 FS Chemistry Systems for the qualitative or semi-quantitative measurement of drugs of abuse.
For in vitro diagnostic use only. VITROS Chemistry Products FS Calibrator 1 is used in conjunction with VITROS Chemistry Products Calibrator Kits to calibrate VITROS 5,1 FS Chemistry Systems.
For in vitro diagnostic use only. VITROS Chemistry Products DAT Performance Verifiers are assayed controls used to monitor performance of urine drugs of abuse screening assays on VITROS 5.1 FS Chemistry Systems.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use _________________________________________________________________________________________________________________________________________________________ (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Caul Benson
vision Sign-Off
Office of In Vitro Diagnostic Device Evaluation and Safety