meddevicedb.com FDA Device Reference

CORNING CERTAIN TM

K820873 Class I Traditional
Decision Date
1982-04-16
Sponsor / Applicant
Corning Medical & Scientific

Technical Specification

510(k) Submission ID K820873
Product Code JJS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1982-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORNING CERTAIN TM received FDA 510(k) clearance under submission number K820873, 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 1982-04-16.

Classification & Regulation

This clearance is catalogued under FDA product code JJS and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.