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ACRO BIOTECH LLC RAPID OPIATES URINE TEST; CATALOG# OPI00100

K053037 Class II Traditional
Decision Date
2006-06-15
Sponsor / Applicant
Acro Biotech, LLC

Technical Specification

510(k) Submission ID K053037
Product Code DJG
Medical Specialty / Panel Clinical Toxicology
Regulation Citation 21 CFR 862.3650
Decision Date 2006-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACRO BIOTECH LLC RAPID OPIATES URINE TEST; CATALOG# OPI00100 received FDA 510(k) clearance under submission number K053037, sponsored by Acro Biotech, LLC. 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 2006-06-15.

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.