510(k) K990552

IMMUNOGLOBULIN A TEST SYSTEM by Dade Behring, Inc. — Product Code CFQ

K990552 is an FDA 510(k) premarket notification submitted by Dade Behring, Inc. for the device "IMMUNOGLOBULIN A TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on March 25, 1999. The device falls under product code CFQ (Radioimmunoassay, Immunoglobulins (G, A, M)), a Class II device regulated under 21 CFR 866.5510. Dade Behring, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 25, 1999
Date Received
February 22, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Immunoglobulins (G, A, M)
Device Class
Class II
Regulation Number
866.5510
Review Panel
IM
Submission Type