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RAICHEM MULTI-ANALYTE CALIBRATOR

K012250 Class II Abbreviated
Decision Date
2001-09-24
Sponsor / Applicant
Hemagen Diagnostics, Inc.

Technical Specification

510(k) Submission ID K012250
Product Code JIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2001-09-24
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RAICHEM MULTI-ANALYTE CALIBRATOR received FDA 510(k) clearance under submission number K012250, sponsored by Hemagen Diagnostics, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2001-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code JIX and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.