meddevicedb.com FDA Device Reference

QUICKPAC II ONE STEP COCAINE TEST

K992990 Class II Traditional
Decision Date
1999-09-20
Sponsor / Applicant
Syntron Bioresearch, Inc.

Technical Specification

510(k) Submission ID K992990
Product Code DIO
Medical Specialty / Panel Clinical Toxicology
Regulation Citation 21 CFR 862.3250
Decision Date 1999-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUICKPAC II ONE STEP COCAINE TEST received FDA 510(k) clearance under submission number K992990, sponsored by Syntron Bioresearch, 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 1999-09-20.

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.