meddevicedb.com FDA Device Reference

STRATUS CS ACUTE CARE CARDIOPHASE HSCRP TESTPAK

K062924 Class II Traditional
Decision Date
2006-12-26
Sponsor / Applicant
Dade Behring, Inc.

Technical Specification

510(k) Submission ID K062924
Product Code NQD
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2006-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRATUS CS ACUTE CARE CARDIOPHASE HSCRP TESTPAK received FDA 510(k) clearance under submission number K062924, sponsored by Dade Behring, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2006-12-26.

Classification & Regulation

This clearance is catalogued under FDA product code NQD and 21 CFR 866.5270, within the Immunology review panel as a Class II device.