Parker Hannifin Corp. is one of 25984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Parker Hannifin Corp. - FDA 510(k) Cleared Devices
Recent clearances: Cleveland Multiport Ventricular Catheter Set, PARKER AMBULATORY MEDICATION INFUSION PUMP 2004, MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSER
8
Total
8
Cleared
0
Denied
Parker Hannifin Corp. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 8 cleared submissions from 1983 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Parker Hannifin Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Parker Hannifin Corp.
8 devices
Cleared
Mar 27, 2017
Cleveland Multiport Ventricular Catheter Set
Neurology
277d
Cleared
Sep 28, 1990
PARKER AMBULATORY MEDICATION INFUSION PUMP 2004
General Hospital
282d
Cleared
Jan 14, 1987
MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSER
General Hospital
127d
Cleared
Jan 30, 1984
MODEL 2000 AMBULATORY MED. INFUSER
General Hospital
98d
Cleared
Jan 30, 1984
INFUSION PUMP PRIMER
General Hospital
42d
Cleared
Aug 08, 1983
PRESSURE MONITOR & CONTROL UNIT APC-02A
Gastroenterology & Urology
98d
Cleared
Jun 30, 1983
PLASMA THERAPY TUBESET-E100 SERIES
Hematology
29d
Cleared
Apr 12, 1983
ASAHI BLOOD/PLASMA PUMP #ABP-01A &
Gastroenterology & Urology
28d