MICRO-STRIP FOR AMPHETAMINE METABOLITES

K974611 · Microdiagnostics, Inc. · DKZ · Mar 20, 1998 · Clinical Toxicology

Device Facts

• Record ID: K974611
• Device Name: MICRO-STRIP FOR AMPHETAMINE METABOLITES
• Applicant: Microdiagnostics, Inc.
• Product Code: DKZ · Clinical Toxicology
• Decision Date: Mar 20, 1998
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 862.3100
• Device Class: Class 2

Intended Use

The Microdiagnostics, Inc. Micro-Strip for Amphetamine Metabolites is intended to qualitatively detect the metabolites of Amphetamine and Amphetamine-like drugs in urine.

Device Story

Micro-Strip for Amphetamine Metabolites is an in vitro diagnostic test for qualitative detection of amphetamine and amphetamine-like drug metabolites in urine. Device utilizes immunochromatographic assay technology; sample applied to test strip; presence of metabolites indicated by visual color change. Intended for use by healthcare professionals in clinical settings to assist in drug screening. Results provide preliminary analytical test information; clinical consideration and professional judgment required for interpretation. Benefits include rapid, point-of-care identification of potential amphetamine exposure.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Immunochromatographic test strip for qualitative detection of drug metabolites in urine. Visual readout mechanism. In vitro diagnostic device.

Indications for Use

Indicated for the qualitative detection of amphetamine and amphetamine-like drug metabolites in human urine samples.

Regulatory Classification

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.

Special Controls

*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).

Submission Summary (Full Text)

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Food and Drug Administration 2098 Gaither Road Rockville MD 20850

MAR 20 1998

Roy Chung President Microdiagnostics, Inc. 28062 Forbes Road, Suite B Laquna Niquel, California 92677

Re: K974611 Micro-Strip for Amphetamine Metabolites Requlatory Class: II Product Code: DKZ Dated: February 24, 1998 Received: March 2, 1998

Dear Mr. Chung:

We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act 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 (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory In addition, FDA may publish further announcements action. concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.

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Under the Clinical Laboratory Improvement Amendments of 1988 (CLIA-88), this device may require a CLIA complexity categorization. To determine if it does, you should contact the Centers for Disease Control and Prevention (CDC) at [phone].

This letter will allow you to begin marketing your device as described in your 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 advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number [phone] or [phone] or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".

Sincerely yours,
Steven Litman

Steven I. Gutman, M.D., M.B.A. Director Division of Clinical Laboratory Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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510(k) Number (if known):_____________________________________________________________________________________________________________________________________________________

Device Name: Micro-Strip for Amphetamine Metabolites Indications For Use:

The Microdiagnostics, Inc. Micro-Strip for Amphetamine Metabolites is intended to qualitatively detect the metabolites of Amphetamine and Amphetamine-like drugs in urine.

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Concurrence of CDRH, Office of Device Evaluation (ODE)

rescription Use er 21 CFR 801.1091

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Over-The-Counter Use_

(Optional Format 1-2-96)

(Division Sign-Off)
Division of Dental Devices
510(k) Number: K974611