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EDC/TITAN GELISO-TOTAL CPK ISOENZYME PROCEDURE

K852392 Class II Traditional
Decision Date
1985-10-22
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K852392
Product Code CGS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1985-10-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EDC/TITAN GELISO-TOTAL CPK ISOENZYME PROCEDURE received FDA 510(k) clearance under submission number K852392, sponsored by Helena Laboratories. 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 1985-10-22.

Classification & Regulation

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