ClearanceBrief
Company ยท US

Parker Hannifin Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 2024. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FRNPump, Infusion4
PHLPowered Exoskeleton3
BZRMixer, Breathing Gases, Anesthesia Inhalation2
CBNApparatus, Gas-Scavenging1
FIRPump, Blood, Extra-Luminal1
FJKSet, Tubing, Blood, With And Without Anti-Regurgitation Valve1
HCACatheter, Ventricular1
KXMSystem Accessories, Extracorporeal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 19, 2024K241465Midas Flowmeter; eAVS
Parker Hannifin Corporation
BZR
Mar 5, 2023K223452Nitronox Scavenger Plus
Parker Hannifin Corporation
CBN
Apr 22, 2021K202480Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50
Parker Hannifin
BZR
Jan 31, 2018K173530Indego(R)
Parker-Hannifin Corporation
PHL
Sep 8, 2017K171334Indego
Parker Hannifin Corporation
PHL
Mar 27, 2017K161731Cleveland Multiport Ventricular Catheter Set
Parker Hannifin Corp.
HCA
Feb 26, 2016K152416Indego
Parker Hannifin Corporation
PHL
Sep 28, 1990K897086PARKER AMBULATORY MEDICATION INFUSION PUMP 2004
Parker Hannifin Corp.
FRN
Jan 14, 1987K863532MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSER
Parker Hannifin Corp.
FRN
Jan 30, 1984K834461INFUSION PUMP PRIMER
Parker Hannifin Corp.
FRN
Jan 30, 1984K833723MODEL 2000 AMBULATORY MED. INFUSER
Parker Hannifin Corp.
FRN
Aug 8, 1983K831402PRESSURE MONITOR & CONTROL UNIT APC-02A
Parker Hannifin Corp.
KXM
Jun 30, 1983K831747PLASMA THERAPY TUBESET-E100 SERIES
Parker Hannifin Corp.
FJK
Apr 12, 1983K830818ASAHI BLOOD/PLASMA PUMP #ABP-01A &
Parker Hannifin Corp.
FIR

Latest recalls

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