510(k) K840222

CORNING IMMO PHASE FREE T3 by Corning Medical & Scientific — Product Code CDP

K840222 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "CORNING IMMO PHASE FREE T3". The FDA issued a decision of Substantially Equivalent on May 7, 1984. The device falls under product code CDP (Radioimmunoassay, Total Triiodothyronine), a Class II device regulated under 21 CFR 862.1710. Corning Medical & Scientific has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 7, 1984
Date Received
January 19, 1984
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