510(k) K840461

MAGIC 125I DIGOXIN RADIOIMMUNOASSAY by Corning Medical & Scientific — Product Code DON

K840461 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "MAGIC 125I DIGOXIN RADIOIMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on March 23, 1984. The device falls under product code DON (Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.), a Class II device regulated under 21 CFR 862.3320. Corning Medical & Scientific has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 1984
Date Received
February 2, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.
Device Class
Class II
Regulation Number
862.3320
Review Panel
TX
Submission Type