510(k) K961490

ELECSYS T4 ASSAY by Boehringer Mannheim Corp. — Product Code CDX

K961490 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "ELECSYS T4 ASSAY". The FDA issued a decision of Substantially Equivalent on June 13, 1996. The device falls under product code CDX (Radioimmunoassay, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 13, 1996
Date Received
April 18, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Total Thyroxine
Device Class
Class II
Regulation Number
862.1700
Review Panel
CH
Submission Type