Data / Medical devices / United States / Chabner XRT, LLC
Chabner XRT, LLC: FDA-registered device maker in Port Chester, NY, United States, 1 510(k) clearance
Chabner XRT, LLC is registered with the FDA (registration 3030077501) in Port Chester, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 14, 2013. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3030077501
- Address
- 36 Midland Ave, Port Chester, NY, United States, 10573
- Owner or operator
- Chabner XRT, LLC (10089364)
- Roles
- Manufacturer
- First device listed
- December 1, 2023
- Registered through
- 2027
- Brand names listed
- Chabner XRT
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accelerator, Linear, Medical | IYE | 2 | 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 |
|---|---|---|---|---|---|---|
| June 14, 2013 | K121284 | CHABNER XRT GARMENTS | IYE | Substantially Equivalent | Chabner Xrt, LLC | accessdata.fda.gov |
Compare with other makers
Updated June 14, 2013. 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.