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NORDICLAB TOTAL ESTRIOL RIA TEST

K792189 Class I Traditional
Decision Date
1979-11-13
Sponsor / Applicant
Nordiclab Intl.

Technical Specification

510(k) Submission ID K792189
Product Code CGI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1265
Decision Date 1979-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NORDICLAB TOTAL ESTRIOL RIA TEST received FDA 510(k) clearance under submission number K792189, sponsored by Nordiclab Intl.. 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 1979-11-13.

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.