meddevicedb.com FDA Device Reference

EMBRITROL CK-MB CONTROLS

K812671 Class I Traditional
Decision Date
1981-10-02
Sponsor / Applicant
Intl. Immunoassay Laboratories, Inc.

Technical Specification

510(k) Submission ID K812671
Product Code JJT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1981-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMBRITROL CK-MB CONTROLS received FDA 510(k) clearance under submission number K812671, sponsored by Intl. Immunoassay Laboratories, Inc.. 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 1981-10-02.

Classification & Regulation

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