510(k) K896991

ENZYMUN TEST(R) TBK by Boehringer Mannheim Corp. — Product Code CEE

K896991 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "ENZYMUN TEST(R) TBK". The FDA issued a decision of Substantially Equivalent on March 1, 1990. The device falls under product code CEE (Radioimmunoassay, Thyroxine-Binding Globulin), a Class II device regulated under 21 CFR 862.1685. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 1, 1990
Date Received
December 13, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Thyroxine-Binding Globulin
Device Class
Class II
Regulation Number
862.1685
Review Panel
CH
Submission Type