Medical Device Manufacturer · US , Walker , MI

Parker Hannifin Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1983

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) cleared devices by Parker Hannifin Corp.

8 devices

1-8 of 8

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