510(k) K963127

ELECSYS FT3 by Boehringer Mannheim Corp. — Product Code CDP

K963127 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "ELECSYS FT3". The FDA issued a decision of Substantially Equivalent on December 16, 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
December 16, 1996
Date Received
August 12, 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