meddevicedb.com FDA Device Reference

ELECSYS PRECICONTROL TROPONIN T

K031990 Class I Traditional
Decision Date
2003-08-20
Sponsor / Applicant
Roche Diagnostics Corp.

Technical Specification

510(k) Submission ID K031990
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2003-08-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECSYS PRECICONTROL TROPONIN T received FDA 510(k) clearance under submission number K031990, sponsored by Roche Diagnostics 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 2003-08-20.

Classification & Regulation

This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.