510(k) K010864

ANALYST PANELS + ANALYTICAL TEST ROTOR by Hemagen Diagnostics, Inc. — Product Code KHS

K010864 is an FDA 510(k) premarket notification submitted by Hemagen Diagnostics, Inc. for the device "ANALYST PANELS + ANALYTICAL TEST ROTOR". The FDA issued a decision of Substantially Equivalent on May 21, 2001. The device falls under product code KHS (Enzymatic, Carbon-Dioxide), a Class II device regulated under 21 CFR 862.1160. Hemagen Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 21, 2001
Date Received
March 22, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzymatic, Carbon-Dioxide
Device Class
Class II
Regulation Number
862.1160
Review Panel
CH
Submission Type