meddevicedb.com FDA Device Reference

ADVIA Centaur High-Sensitivity Troponin I (TNIH)

K171274 Class II Traditional
Decision Date
2018-07-12
Sponsor / Applicant
Siemens Healthcare Diagnostics, Inc.

Technical Specification

510(k) Submission ID K171274
Product Code MMI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 2018-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVIA Centaur High-Sensitivity Troponin I (TNIH) received FDA 510(k) clearance under submission number K171274, sponsored by Siemens Healthcare 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 2018-07-12.

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.