meddevicedb.com FDA Device Reference

CPK ISOENZYME CONTROL

K791299 Class I Traditional
Decision Date
1979-08-16
Sponsor / Applicant
Electrophoresis Corp. of America

Technical Specification

510(k) Submission ID K791299
Product Code JJT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1979-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CPK ISOENZYME CONTROL received FDA 510(k) clearance under submission number K791299, sponsored by Electrophoresis Corp. of America. 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 1979-08-16.

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.