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DIRECT TESTOSTERONE RIA

K811536 Class I Traditional
Decision Date
1981-06-18
Sponsor / Applicant
Immuchem Corp.

Technical Specification

510(k) Submission ID K811536
Product Code CDZ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1680
Decision Date 1981-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIRECT TESTOSTERONE RIA received FDA 510(k) clearance under submission number K811536, sponsored by Immuchem Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1981-06-18.

Classification & Regulation

This clearance is catalogued under FDA product code CDZ and 21 CFR 862.1680, within the Clinical Chemistry review panel as a Class I device.