Parke-Davis Co. - FDA 510(k) Cleared Devices
47
Total
47
Cleared
0
Denied
FDA 510(k) Regulatory Record - Parke-Davis Co. Cardiovascular ✕
12 devices
Cleared
Aug 29, 1986
DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR
Cardiovascular
87d
Cleared
Mar 31, 1986
ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE
Cardiovascular
45d
Cleared
Aug 19, 1985
DESERET THERMODILUTION CARDIAC OUTPUT
Cardiovascular
461d
Cleared
May 16, 1985
DESERET INTRODUCER SET
Cardiovascular
155d
Cleared
Aug 06, 1984
DESERET DISPOSABLE PRESSURE TRANSDUCER
Cardiovascular
83d
Cleared
Jun 11, 1984
DESERET HEPARIN COATED FLOW CATH
Cardiovascular
77d
Cleared
Jun 11, 1984
DESERET HEPARIN COATED FLOW DIRECTED
Cardiovascular
70d
Cleared
Jan 13, 1984
DESERET EPIDURAL CATHETER
Cardiovascular
24d
Cleared
Sep 12, 1983
ANGIO-FLO CONTIN-ARTERIAL FLUSH DEV.
Cardiovascular
77d
Cleared
Jan 27, 1983
INTRACATH-DA INTRAVENOUS CATH. PLACEMENT
Cardiovascular
101d
Cleared
Dec 15, 1982
INTRA CATH-DSA INTRAVENOUS CATH PLACE.
Cardiovascular
58d
Cleared
Jul 16, 1976
SURGICAL BLADES (BEAVER)
Cardiovascular
35d