FDA applicant

Parker Hannifin Corp.

Walker, MI14 decisions1983–20240 recalls

FDA records 14 decisions for Parker Hannifin Corp. (Walker, MI) from 1983 to 2024: 14 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and PHL (Powered Exoskeleton). Its devices cite 12 predicates, 3 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Parker Hannifin Corporation”, “Parker Hannifin”, “Parker-Hannifin Corporation”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Parker Hannifin Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2007high 2 (2017) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Parker Hannifin Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Parker Hannifin Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Parker”

FDA records each applicant name separately; these may or may not be the same firm.

Parker Laboratories, Inc. 30 Parker Treadmill Co., Inc. 2 Parker Medical Assoc. 1

Parker Hannifin Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Parker”