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LIFESIGN MI MYOGLOBIN/TROPONIN I RAPID TEST

K022946 Class II Traditional
Decision Date
2002-10-08
Sponsor / Applicant
Princeton BioMeditech Corp.

Technical Specification

510(k) Submission ID K022946
Product Code MMI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 2002-10-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFESIGN MI MYOGLOBIN/TROPONIN I RAPID TEST received FDA 510(k) clearance under submission number K022946, sponsored by Princeton BioMeditech Corp.. 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 2002-10-08.

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.