Parke-Davis Co. - FDA 510(k) Cleared Devices
Recent clearances: INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT, DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR, ATI DISPOSABLE BIOLOGICAL TEST PACK
47
Total
47
Cleared
0
Denied
FDA 510(k) Regulatory Record - Parke-Davis Co. General Hospital ✕
22 devices
Cleared
Dec 04, 1986
INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT
General Hospital
212d
Cleared
Jun 18, 1986
ATI DISPOSABLE BIOLOGICAL TEST PACK
General Hospital
177d
Cleared
Mar 18, 1986
VIAPIC CENTRAL LINE CATHETER
General Hospital
49d
Cleared
Nov 01, 1985
DISPOSABLE STEAM BIOLOGICAL TEST PACK
General Hospital
165d
Cleared
Jun 14, 1985
DESERET ARTERIAL CATHETER
General Hospital
71d
Cleared
Jun 07, 1985
SPECTRUM(TENTATIVE)
General Hospital
25d
Cleared
Dec 03, 1984
DESERET INTRAVASCULAR CATHETER
General Hospital
124d
Cleared
Nov 28, 1984
DESERET SUBCLAVIAN JUGULAR CATHETER SET
General Hospital
36d
Cleared
Nov 28, 1984
DESERET DENTRAL LINE CATHETER
General Hospital
28d
Cleared
May 09, 1984
STERILIZATION PROCESS INDICATOR
General Hospital
51d
Cleared
Apr 17, 1984
DESERET LONG TERM INDWELLING CATHETER
General Hospital
42d
Cleared
Mar 22, 1984
DESERET INFANT CENTRAL VENOUS CATHE-
General Hospital
71d