meddevicedb.com FDA Device Reference

BAYER HEALTHCARE RAPIDQC PLUS

K870036 Class I Traditional
Decision Date
1987-01-14
Sponsor / Applicant
Ciba Corning Diagnostics Corp.

Technical Specification

510(k) Submission ID K870036
Product Code JJS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1987-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAYER HEALTHCARE RAPIDQC PLUS received FDA 510(k) clearance under submission number K870036, sponsored by Ciba Corning Diagnostics 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 1987-01-14.

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.