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CLOTRAC HEPARINASE TEST CARTIDGE (HTC) COAGULATION CONTROL

K103314 Class II Special
Decision Date
2010-12-03
Sponsor / Applicant
Medtronic, Inc.

Technical Specification

510(k) Submission ID K103314
Product Code GGN
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5425
Decision Date 2010-12-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLOTRAC HEPARINASE TEST CARTIDGE (HTC) COAGULATION CONTROL received FDA 510(k) clearance under submission number K103314, sponsored by Medtronic, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2010-12-03.

Classification & Regulation

This clearance is catalogued under FDA product code GGN and 21 CFR 864.5425, within the Hematology review panel as a Class II device.