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AQ ONE STEP COCAINE TEST

K972384 Class II Traditional
Decision Date
1997-08-06
Sponsor / Applicant
Bionike Laboratories, Inc.

Technical Specification

510(k) Submission ID K972384
Product Code DIO
Medical Specialty / Panel Clinical Toxicology
Regulation Citation 21 CFR 862.3250
Decision Date 1997-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AQ ONE STEP COCAINE TEST received FDA 510(k) clearance under submission number K972384, sponsored by Bionike Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Toxicology review panel. The statutory decision date of record is 1997-08-06.

Classification & Regulation

This clearance is catalogued under FDA product code DIO and 21 CFR 862.3250, within the Clinical Toxicology review panel as a Class II device.