meddevicedb.com FDA Device Reference

CIBA CORNING MAGIC(R) LITE CKMB IMMUNOASSAY

K870987 Class II Traditional
Decision Date
1987-05-26
Sponsor / Applicant
Ciba Corning Diagnostics Corp.

Technical Specification

510(k) Submission ID K870987
Product Code JHX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1987-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIBA CORNING MAGIC(R) LITE CKMB IMMUNOASSAY received FDA 510(k) clearance under submission number K870987, 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 1987-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code JHX and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.