510(k) K961488

ELECSYS T-UPTAKE ASSAY by Boehringer Mannheim Corp. — Product Code KHQ

K961488 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "ELECSYS T-UPTAKE ASSAY". The FDA issued a decision of Substantially Equivalent on June 12, 1996. The device falls under product code KHQ (Radioassay, Triiodothyronine Uptake), a Class II device regulated under 21 CFR 862.1715. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 12, 1996
Date Received
April 18, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioassay, Triiodothyronine Uptake
Device Class
Class II
Regulation Number
862.1715
Review Panel
CH
Submission Type