meddevicedb.com FDA Device Reference

COAG-1 PT-NC TEST CARD

K904325 Class II Traditional
Decision Date
1991-01-25
Sponsor / Applicant
Cardiovascular Diagnostic Services

Technical Specification

510(k) Submission ID K904325
Product Code GJS
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7750
Decision Date 1991-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COAG-1 PT-NC TEST CARD received FDA 510(k) clearance under submission number K904325, sponsored by Cardiovascular Diagnostic Services. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1991-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code GJS and 21 CFR 864.7750, within the Hematology review panel as a Class II device.