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CARDIO REP-CAT. NO. 1400 & CK ISOFORMS KIT 3305

K930359 Class II Traditional
Decision Date
1993-04-12
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K930359
Product Code JHT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1993-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARDIO REP-CAT. NO. 1400 & CK ISOFORMS KIT 3305 received FDA 510(k) clearance under submission number K930359, 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 1993-04-12.

Classification & Regulation

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