Data / Medical devices / United States / P4X Inc
P4X Inc: FDA-registered device maker in Grand Prairie, TX, United States, 1 510(k) clearance
P4X Inc is registered with the FDA (registration 3004013215) in Grand Prairie, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 31, 2003. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3004013215
- Address
- 2374 NW Dallas ST, Grand Prairie, TX, United States, 75050
- Owner or operator
- P4X Inc. DBA Per4max Medical (9055719)
- Roles
- Manufacturer
- First device listed
- September 9, 2016
- Registered through
- 2027
- Brand names listed
- p4x inc
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Mechanical | IOR | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 31, 2003 | K032123 | SHOCKWAVE SUSPENSION WHEELCHAIR | IOR | Substantially Equivalent | Per4max Medical, LLC | accessdata.fda.gov |
Compare with other makers
Updated July 31, 2003. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.