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CARESTART CARDIAC 3-IN-1 TROPONIN 1/CK-MB/MYOGLOBIN

K051925 Class II Traditional
Decision Date
2005-11-29
Sponsor / Applicant
Access Bio Incorporate

Technical Specification

510(k) Submission ID K051925
Product Code MMI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 2005-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARESTART CARDIAC 3-IN-1 TROPONIN 1/CK-MB/MYOGLOBIN received FDA 510(k) clearance under submission number K051925, sponsored by Access Bio Incorporate. 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 2005-11-29.

Classification & Regulation

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