Parker Hannifin Corp.

Macedonia, OH, US

Parker Hannifin Corp. appears in FDA device records in Macedonia, OH. FDA records list 14 510(k) clearances between 1983-04-12 and 2024-09-19, no PMA records and no registered establishments. As of 2026-09-10, FDA records show no recalls for this company.

510(k) clearances: 14
PMA records: 0
Recall records: 0
Registered establishments: 0

510(k) clearance history

FDA records hold 14 510(k) clearances for Parker Hannifin Corp. between 1983 and 2024. The busiest year on record is 1983, with 3. The most recent is 2024, with 1.

Clearances by year, as a table

510(k) clearance decisions for Parker Hannifin Corp., by decision year
Year	Clearances
1983	3
1984	2
1987	1
1990	1
2016	1
2017	2
2018	1
2021	1
2023	1
2024	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K241465	Midas Flowmeter; eAVS	BZR	Substantially Equivalent	2024-09-19
K223452	Nitronox Scavenger Plus	CBN	Substantially Equivalent	2023-03-05
K202480	Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50	BZR	Substantially Equivalent	2021-04-22
K173530	Indego(R)	PHL	Substantially Equivalent	2018-01-31
K171334	Indego	PHL	Substantially Equivalent	2017-09-08
K161731	Cleveland Multiport Ventricular Catheter Set	HCA	Substantially Equivalent	2017-03-27
K152416	Indego	PHL	Substantially Equivalent	2016-02-26
K897086	PARKER AMBULATORY MEDICATION INFUSION PUMP 2004	FRN	Substantially Equivalent	1990-09-28
K863532	MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSER	FRN	Substantially Equivalent	1987-01-14
K834461	INFUSION PUMP PRIMER	FRN	Substantially Equivalent	1984-01-30
K833723	MODEL 2000 AMBULATORY MED. INFUSER	FRN	Substantially Equivalent	1984-01-30
K831402	PRESSURE MONITOR & CONTROL UNIT APC-02A	KXM	Substantially Equivalent	1983-08-08
K831747	PLASMA THERAPY TUBESET-E100 SERIES	FJK	Substantially Equivalent	1983-06-30
K830818	ASAHI BLOOD/PLASMA PUMP #ABP-01A &	FIR	Substantially Equivalent	1983-04-12

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain