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HEMOSIL SPECIAL TEST CONTROLS LEVEL 1 & 2

K040359 Class II Traditional
Decision Date
2004-03-19
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K040359
Product Code JPA
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5425
Decision Date 2004-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOSIL SPECIAL TEST CONTROLS LEVEL 1 & 2 received FDA 510(k) clearance under submission number K040359, sponsored by Instrumentation Laboratory CO. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2004-03-19.

Classification & Regulation

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