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THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY

K041502 Class II Traditional
Decision Date
2004-09-01
Sponsor / Applicant
Haemoscope Corp.

Technical Specification

510(k) Submission ID K041502
Product Code JOZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5700
Decision Date 2004-09-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY received FDA 510(k) clearance under submission number K041502, sponsored by Haemoscope 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 2004-09-01.

Classification & Regulation

This clearance is catalogued under FDA product code JOZ and 21 CFR 864.5700, within the Hematology review panel as a Class II device.