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GAMMADAB B-HCG RADIOIMMUNOASSAY KIT

K801409 Class II Traditional
Decision Date
1980-07-14
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K801409
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1980-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GAMMADAB B-HCG RADIOIMMUNOASSAY KIT received FDA 510(k) clearance under submission number K801409, sponsored by Travenol Laboratories, S.A.. 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 1980-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code JHI and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.