510(k) K770365

RADIOIMMUNOASSAY DIGOXIN TEST, IN VITRO by Travenol Laboratories, S.A. — Product Code DPO

K770365 is an FDA 510(k) premarket notification submitted by Travenol Laboratories, S.A. for the device "RADIOIMMUNOASSAY DIGOXIN TEST, IN VITRO". The FDA issued a decision of Substantially Equivalent on February 24, 1977. The device falls under product code DPO (Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep.), a Class II device regulated under 21 CFR 862.3320. Travenol Laboratories, S.A. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1977
Date Received
February 23, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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