510(k) K945642

AGEN DIMERTEST GOLD EIA by Agen Biomedical , Ltd. — Product Code GHH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 1995
Date Received
November 16, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fibrin Split Products
Device Class
Class II
Regulation Number
864.7320
Review Panel
HE
Submission Type