Healgen Multi-Drug Urine Test Cup; Healgen Multi-Drug Urine Test Dip Card

K163704 · Healgen Scientific,, LLC · JXM · Aug 2, 2017 · Clinical Toxicology

Device Facts

Record IDK163704
Device NameHealgen Multi-Drug Urine Test Cup; Healgen Multi-Drug Urine Test Dip Card
ApplicantHealgen Scientific,, LLC
Product CodeJXM · Clinical Toxicology
Decision DateAug 2, 2017
DecisionSESE
Submission TypeSpecial
Regulation21 CFR 862.3170
Device ClassClass 2

Indications for Use

The Healgen Drug Test Cup and Dipcard are lateral flow chromatographic immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine at the following cut-off concentrations: Amphetamine (AMP) 1000 ng/mL, Secobarbital (BAR) 300 ng/mL, Buprenorphine (BUP) 10 ng/mL, Cocaine (COC) 300 ng/mL, Methamphetamine (MET) 1000 ng/mL, Methylenedioxymethamphetamine (MDMA) 500 ng/mL, Methadone (MTD) 300 ng/mL, Morphine (MOP) 300 ng/mL, Nortriptyline (TCA) 1000 ng/mL, Oxazepam (OPI) 300 ng/mL, Phencyclidine (PCP) 25 ng/mL, Propoxyphene (PPX) 300 ng/mL, Marijuana (THC) 50 ng/mL, and Oxycodone (OXY) 100 ng/mL. The device is intended for healthcare professional use, including professional use at point-of-care sites, to assist in the determination of drug compliance. It is not intended for over-the-counter sale. The device provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) or liquid chromatography/tandem mass spectrometry (LC/MS/MS) are the preferred confirmatory methods. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

Device Story

Lateral flow immunochromatographic assay for qualitative detection of drugs of abuse in human urine. Device uses competitive binding principle; drug-free samples or samples below cutoff generate colored line in test region; positive samples (at or above cutoff) do not. Control line always appears. Available as multi-drug test cup or dip card (2-14 analytes). Used by lay users (OTC) or clinicians (prescription) for preliminary screening. Results require confirmation via GC/MS or LC/MS. Benefits include rapid, simultaneous screening for multiple substances to support clinical decision-making.

Clinical Evidence

Lay-user study conducted at three sites with 300 participants per format (ages 20 to >50). Samples spiked with drugs at negative, +/-75%, +/-50%, +/-25% of cutoff concentrations, confirmed by GC/MS. Results showed high percentage agreement across all analytes and concentrations. Flesch-Kincaid analysis of package inserts indicated a Grade Level of 7, confirming ease of use for lay persons.

Technological Characteristics

Lateral flow chromatographic immunoassay. Format: multi-drug test cup and dipcard. Analyte detection via competitive binding principle. Qualitative visual readout. No electronic components, software, or energy source required.

Indications for Use

Indicated for qualitative, simultaneous detection of drugs of abuse (Amphetamine, Oxazepam, Cocaine, Cannabinoids, Methamphetamine, Morphine, Oxycodone, Secobarbital, Buprenorphine, MDMA, Phencyclidine, Propoxyphene, Nortriptyline, Methadone) in human urine. Intended for both prescription and OTC use. Not for distinguishing between prescription use and abuse.

Regulatory Classification

Identification

A benzodiazepine test system is a device intended to measure any of the benzodiazepine compounds, sedative and hypnotic drugs, in blood, plasma, and urine. The benzodiazepine compounds include chlordiazepoxide, diazepam, oxazepam, chlorzepate, flurazepam, and nitrazepam. Measurements obtained by this device are used in the diagnosis and treatment of benzodiazepine use or overdose and in monitoring levels of benzodiazepines to ensure appropriate therapy.

Special Controls

*Classification.* Class II (special controls). A benzodiazepine 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).

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0} SPECIAL 510(k): Device Modification OIR Decision Summary To: THE FILE RE: DOCUMENT NUMBER k163704 This 510(k) submission contains information/data on modifications made to the SUBMITTER'S own Class II, Class III or Class I devices requiring 510(k). The following items are present and acceptable (delete/add items as necessary): 1. The name and 510(k) number of the SUBMITTER'S previously cleared device. (For a preamendments device, a statement to this effect has been provided.) k142280 Healgen Oxazepam and Morphine Tests k143187 Healgen Amphetamine and Oxycodone Tests k141647 Healgen Cocaine Test k140546 Healgen Marijuana and Methamphetamine Tests k150791 Healgen Secobarbital, Buprenorphine, and Methadone Tests k150096 Healgen MDMA and Phencyclidine Tests k151348 Healgen Nortriptyline, Propoxyphene, and EDDP Tests k152269 Healgen Amphetamine, Cocaine, and Methamphetamine Tests 2. Submitter's statement that the INDICATION/INTENDED USE of the modified device as described in its labeling HAS NOT CHANGED along with the proposed labeling which includes instructions for use, package labeling, and, if available, advertisements or promotional materials (labeling changes are permitted as long as they do not affect the intended use). 3. A description of the device MODIFICATION(S), including clearly labeled diagrams, engineering drawings, photographs, user's and/or service manuals in sufficient detail to demonstrate that the FUNDAMENTAL SCIENTIFIC TECHNOLOGY of the modified device has not changed. This change was for the combination of fourteen previously cleared assays (test strips) into a single device in cup and dipcard formats. 4. Comparison Information (similarities and differences) to applicant's legally marketed predicate device including, labeling, intended use, physical characteristics, and cutoffs. 5. A Design Control Activities Summary which includes: a) Identification of Risk Analysis method(s) used to assess the impact of the modification on the device and its components, and the results of the analysis b) Based on the Risk Analysis, an identification of the verification and/or validation activities required, including methods or tests used and acceptance criteria to be applied The labeling for this modified subject device has been reviewed to verify that the indication/intended use for the device is unaffected by the modification. In addition, the submitter's description of the particular modification(s) and the comparative information between the modified and unmodified devices demonstrate that the fundamental scientific technology has not changed. The submitter has provided the design control information as specified in The New 510(k) Paradigm and on this basis, I {1} recommend the device be determined substantially equivalent to the previously cleared (or their preamendment) device. 2
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