meddevicedb.com FDA Device Reference

ISOCONTROL SERUM CK-MB

K850213 Class I Traditional
Decision Date
1985-03-05
Sponsor / Applicant
Sclavo, Inc.

Technical Specification

510(k) Submission ID K850213
Product Code JJT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1985-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISOCONTROL SERUM CK-MB received FDA 510(k) clearance under submission number K850213, sponsored by Sclavo, 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 1985-03-05.

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.