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VERDICT -II OPIATES 2000

K992111 Class II Traditional
Decision Date
1999-12-16
Sponsor / Applicant
Medtox Diagnostics, Inc.

Technical Specification

510(k) Submission ID K992111
Product Code DJG
Medical Specialty / Panel Clinical Toxicology
Regulation Citation 21 CFR 862.3650
Decision Date 1999-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERDICT -II OPIATES 2000 received FDA 510(k) clearance under submission number K992111, sponsored by Medtox Diagnostics, 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 1999-12-16.

Classification & Regulation

This clearance is catalogued under FDA product code DJG and 21 CFR 862.3650, within the Clinical Toxicology review panel as a Class II device.