# Parker Hannifin Corp.

- Location (FDA's records): Walker, MI
- FDA decisions: 14 (1983–2024): 14 510(k) clearances
- Names in FDA's records: Parker Hannifin Corp. (8); Parker Hannifin Corporation (4); Parker Hannifin (1); Parker-Hannifin Corporation (1)
- Product codes: FRN (4), PHL (3), BZR (2), KXM (1), CBN (1), FIR (1), FJK (1), HCA (1)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 7 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ekso Bionics, Inc.: 2 (https://510kreport.com/company/ekso-bionics)
- Baldus Sedation GmbH & Co. KG: 1 (https://510kreport.com/company/baldus-sedation)
- G. Dundas Co.: 1 (https://510kreport.com/company/g-dundas)
- Fraser Sweatman, Inc.: 1 (https://510kreport.com/company/fraser-sweatman)
- Argo Medical Technologies, Inc.: 1 (https://510kreport.com/company/argo-medical-technologies)
- Mri Interventions, Inc.: 1 (https://510kreport.com/company/mri-interventions)
- Alcyone Lifesciences, Inc.: 1 (https://510kreport.com/company/alcyone-lifesciences)
- Surgivision, Inc.: 1 (https://510kreport.com/company/surgivision)

## Firms that cite its devices most
- Wandercraft SAS: 3 (https://510kreport.com/company/wandercraft)
- Re Walk Robotics, Ltd.: 1 (https://510kreport.com/company/re-walk-robotics)

## Its most-cited devices
- K173530: Indego (R) (2018), cited by 4
- K152416: Indego (2016), cited by 2
- K171334: Indego (2017), cited by 1

## Recent decisions
- K241465: Midas Flowmeter; eAVS (Sep 19, 2024)
- K223452: Nitronox Scavenger Plus (Mar 5, 2023)
- K202480: Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 (Apr 22, 2021)
- K173530: Indego (R) (Jan 31, 2018)
- K171334: Indego (Sep 8, 2017)
- K161731: Cleveland Multiport Ventricular Catheter Set (Mar 27, 2017)
- K152416: Indego (Feb 26, 2016)
- K897086: Parker Ambulatory Medication Infusion Pump 2004 (Sep 28, 1990)

Source page: https://510kreport.com/company/parker-hannifin