510(k) K961236

UBI MAGIWEL TRIIODOTHYRONINE(T3) QUANTITATIVE by United Biotech, Inc. — Product Code CDP

K961236 is an FDA 510(k) premarket notification submitted by United Biotech, Inc. for the device "UBI MAGIWEL TRIIODOTHYRONINE(T3) QUANTITATIVE". The FDA issued a decision of Substantially Equivalent on May 30, 1996. The device falls under product code CDP (Radioimmunoassay, Total Triiodothyronine), a Class II device regulated under 21 CFR 862.1710. United Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 30, 1996
Date Received
March 29, 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