meddevicedb.com FDA Device Reference

PROLACTIN (125) RADIOIMMUNAOASSAY

K803273 Class I Traditional
Decision Date
1981-01-16
Sponsor / Applicant
Corning Medical & Scientific

Technical Specification

510(k) Submission ID K803273
Product Code CFT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1625
Decision Date 1981-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROLACTIN (125) RADIOIMMUNAOASSAY received FDA 510(k) clearance under submission number K803273, sponsored by Corning Medical & Scientific. 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 1981-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code CFT and 21 CFR 862.1625, within the Clinical Chemistry review panel as a Class I device.