510(k) K925988

MULTIFIBREN by Behring Diagnostics, Inc. — Product Code KQJ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 1, 1993
Date Received
November 25, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Fibrinogen Determination
Device Class
Class II
Regulation Number
864.7340
Review Panel
HE
Submission Type