510(k) K012250

RAICHEM MULTI-ANALYTE CALIBRATOR by Hemagen Diagnostics, Inc. — Product Code JIX

K012250 is an FDA 510(k) premarket notification submitted by Hemagen Diagnostics, Inc. for the device "RAICHEM MULTI-ANALYTE CALIBRATOR". The FDA issued a decision of Substantially Equivalent on September 24, 2001. The device falls under product code JIX (Calibrator, Multi-Analyte Mixture), a Class II device regulated under 21 CFR 862.1150. Hemagen Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 24, 2001
Date Received
July 17, 2001
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrator, Multi-Analyte Mixture
Device Class
Class II
Regulation Number
862.1150
Review Panel
CH
Submission Type