meddevicedb.com FDA Device Reference

RIA KIT, GAMMACOAT

K782109 Class II Traditional
Decision Date
1979-01-26
Sponsor / Applicant
Clinical Assays, Inc.

Technical Specification

510(k) Submission ID K782109
Product Code CDX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1979-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RIA KIT, GAMMACOAT received FDA 510(k) clearance under submission number K782109, sponsored by Clinical Assays, Inc.. 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 1979-01-26.

Classification & Regulation

This clearance is catalogued under FDA product code CDX and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.