meddevicedb.com FDA Device Reference

OPUS TROPONIN I

K955284 Class II Traditional
Decision Date
1996-01-25
Sponsor / Applicant
Behring Diagnostics, Inc.

Technical Specification

510(k) Submission ID K955284
Product Code MMI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1996-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPUS TROPONIN I received FDA 510(k) clearance under submission number K955284, sponsored by Behring Diagnostics, Inc.. 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 1996-01-25.

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.