510(k) K911631

PHARMACIA SPECIFIC IGE CONTROL by Pharmacia, Inc. — Product Code DGC

K911631 is an FDA 510(k) premarket notification submitted by Pharmacia, Inc. for the device "PHARMACIA SPECIFIC IGE CONTROL". The FDA issued a decision of Substantially Equivalent on April 24, 1991. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Pharmacia, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 24, 1991
Date Received
April 11, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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