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HEPARIN ASSAY CARTRIDGES AND CONTROLS

K944115 Class II Traditional
Decision Date
1995-03-24
Sponsor / Applicant
Medtronic Hemotec, Inc.

Technical Specification

510(k) Submission ID K944115
Product Code GFT
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7525
Decision Date 1995-03-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEPARIN ASSAY CARTRIDGES AND CONTROLS received FDA 510(k) clearance under submission number K944115, sponsored by Medtronic Hemotec, 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 1995-03-24.

Classification & Regulation

This clearance is catalogued under FDA product code GFT and 21 CFR 864.7525, within the Hematology review panel as a Class II device.