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CLOT 2 SEMIAUTOMATIC COAGULATION ANALYZER

K900685 Class II Traditional
Decision Date
1990-04-16
Sponsor / Applicant
Texas Intl. Laboratories, Inc.

Technical Specification

510(k) Submission ID K900685
Product Code KQG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5400
Decision Date 1990-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLOT 2 SEMIAUTOMATIC COAGULATION ANALYZER received FDA 510(k) clearance under submission number K900685, sponsored by Texas Intl. Laboratories, Inc.. 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 KQG and 21 CFR 864.5400, within the Hematology review panel as a Class II device.