510(k) K962760

ENZYMUN-TEST FT3 by Boehringer Mannheim Corp. — Product Code CDP

K962760 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "ENZYMUN-TEST FT3". The FDA issued a decision of Substantially Equivalent on November 29, 1996. The device falls under product code CDP (Radioimmunoassay, Total Triiodothyronine), a Class II device regulated under 21 CFR 862.1710. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 1996
Date Received
July 16, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Total Triiodothyronine
Device Class
Class II
Regulation Number
862.1710
Review Panel
CH
Submission Type