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HEMOCUE HBA1C 501 GLYCOSYLATED HEMOGLOBIN MONITORING SYSTEM

K141750 Class II Special
Decision Date
2014-07-24
Sponsor / Applicant
Infopia Co, Ltd.

Technical Specification

510(k) Submission ID K141750
Product Code LCP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7470
Decision Date 2014-07-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOCUE HBA1C 501 GLYCOSYLATED HEMOGLOBIN MONITORING SYSTEM received FDA 510(k) clearance under submission number K141750, sponsored by Infopia Co, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2014-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.