meddevicedb.com FDA Device Reference

COAG-A-MATE - RA4

K900895 Class II Traditional
Decision Date
1990-04-16
Sponsor / Applicant
Organon Teknika Corp.

Technical Specification

510(k) Submission ID K900895
Product Code KQJ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7340
Decision Date 1990-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COAG-A-MATE - RA4 received FDA 510(k) clearance under submission number K900895, sponsored by Organon Teknika 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 1990-04-16.

Classification & Regulation

This clearance is catalogued under FDA product code KQJ and 21 CFR 864.7340, within the Hematology review panel as a Class II device.