510(k) K955907

BOEHRINGER MANNHEIM IGA ASSAY by Boehringer Mannheim Corp. — Product Code CZP

K955907 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "BOEHRINGER MANNHEIM IGA ASSAY". The FDA issued a decision of Substantially Equivalent on February 9, 1996. The device falls under product code CZP (Iga, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1996
Date Received
December 29, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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