Parke-Davis Co. - FDA 510(k) Cleared Devices
47
Total
47
Cleared
0
Denied
Parke-Davis Co. has 47 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 47 cleared submissions from 1976 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Parke-Davis Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Parke-Davis Co.
47 devices
Cleared
Dec 04, 1986
INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT
General Hospital
212d
Cleared
Aug 29, 1986
DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR
Cardiovascular
87d
Cleared
Jun 18, 1986
ATI DISPOSABLE BIOLOGICAL TEST PACK
General Hospital
177d
Cleared
Mar 31, 1986
ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE
Cardiovascular
45d
Cleared
Mar 18, 1986
VIAPIC CENTRAL LINE CATHETER
General Hospital
49d
Cleared
Nov 01, 1985
DISPOSABLE STEAM BIOLOGICAL TEST PACK
General Hospital
165d
Cleared
Aug 19, 1985
DESERET THERMODILUTION CARDIAC OUTPUT
Cardiovascular
461d
Cleared
Jun 14, 1985
DESERET ARTERIAL CATHETER
General Hospital
71d
Cleared
Jun 07, 1985
SPECTRUM(TENTATIVE)
General Hospital
25d
Cleared
May 16, 1985
DESERET INTRODUCER SET
Cardiovascular
155d
Cleared
Mar 11, 1985
DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER
Anesthesiology
31d
Cleared
Mar 05, 1985
DESERET EPIDURAL CATHETER
Anesthesiology
28d
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