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TOTAL ESTRIOL RIA KIT

K800036 Class I Traditional
Decision Date
1980-01-21
Sponsor / Applicant
Amersham Corp.

Technical Specification

510(k) Submission ID K800036
Product Code CGI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1265
Decision Date 1980-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL ESTRIOL RIA KIT received FDA 510(k) clearance under submission number K800036, sponsored by Amersham 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 1980-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code CGI and 21 CFR 862.1265, within the Clinical Chemistry review panel as a Class I device.