510(k) K852247

LASER CERULOPLASMIN KIT(CERULOPLASMIN REAGENTS) by Behring Diagnostics, Inc. — Product Code DDB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 10, 1985
Date Received
May 23, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ceruloplasmin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5210
Review Panel
IM
Submission Type