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MEDICA EASYQC HEMATOCRIT CONTROL

K021924 Class II Traditional
Decision Date
2002-06-24
Sponsor / Applicant
Bionostics, Inc.

Technical Specification

510(k) Submission ID K021924
Product Code GLK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 2002-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDICA EASYQC HEMATOCRIT CONTROL received FDA 510(k) clearance under submission number K021924, sponsored by Bionostics, 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 2002-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code GLK and 21 CFR 864.8625, within the Hematology review panel as a Class II device.