meddevicedb.com FDA Device Reference

ROCHE DIAGNOSTICS TINA-QUANT D-DIMER ON COBAS INTEGRA; ROCHE DIAGNOSTICS TINA-QUANT D-DIMER ON HITACHI

K002706 Class II Traditional
Decision Date
2001-03-16
Sponsor / Applicant
Roche Diagnostics Corp.

Technical Specification

510(k) Submission ID K002706
Product Code DAP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7320
Decision Date 2001-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROCHE DIAGNOSTICS TINA-QUANT D-DIMER ON COBAS INTEGRA; ROCHE DIAGNOSTICS TINA-QUANT D-DIMER ON HITACHI received FDA 510(k) clearance under submission number K002706, sponsored by Roche Diagnostics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2001-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code DAP and 21 CFR 864.7320, within the Hematology review panel as a Class II device.