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HemosIL HIT-Ab(PF4-H), HemosIL HIT-Ab(PF4-H) Controls

K153137 Class II Traditional
Decision Date
2016-07-08
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K153137
Product Code LCO
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7695
Decision Date 2016-07-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HemosIL HIT-Ab(PF4-H), HemosIL HIT-Ab(PF4-H) Controls received FDA 510(k) clearance under submission number K153137, 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 2016-07-08.

Classification & Regulation

This clearance is catalogued under FDA product code LCO and 21 CFR 864.7695, within the Hematology review panel as a Class II device.