510(k) K872801

ALLEIA TOTAL IGE EIA W/MONO ANTI. EKIE1, 2, 5 by Diagnostic Products Corp. — Product Code DGO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 10, 1987
Date Received
July 15, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ige, Peroxidase, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5510
Review Panel
PA
Submission Type