Parker Hannifin Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K202480Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50April 22, 2021
K161731Cleveland Multiport Ventricular Catheter SetMarch 27, 2017
K897086PARKER AMBULATORY MEDICATION INFUSION PUMP 2004September 28, 1990
K863532MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSERJanuary 14, 1987
K833723MODEL 2000 AMBULATORY MED. INFUSERJanuary 30, 1984
K834461INFUSION PUMP PRIMERJanuary 30, 1984
K831402PRESSURE MONITOR & CONTROL UNIT APC-02AAugust 8, 1983
K831747PLASMA THERAPY TUBESET-E100 SERIESJune 30, 1983
K830818ASAHI BLOOD/PLASMA PUMP #ABP-01A &April 12, 1983