meddevicedb.com FDA Device Reference

PSYCHEMEDICS OPIATES EIA

K111926 Class II Traditional
Decision Date
2012-05-01
Sponsor / Applicant
Psychemedics Corp.

Technical Specification

510(k) Submission ID K111926
Product Code DJG
Medical Specialty / Panel Clinical Toxicology
Regulation Citation 21 CFR 862.3650
Decision Date 2012-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PSYCHEMEDICS OPIATES EIA received FDA 510(k) clearance under submission number K111926, sponsored by Psychemedics Corp.. 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 2012-05-01.

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.