Data / Medical devices / United States / The University of Texas MD Anderson Cancer Center, Department of Radiation Physics, Division of Radiation Oncology
The University of Texas MD Anderson Cancer Center, Department of Radiation Physics, Division of Radiation Oncology: FDA-registered device maker in Houston, TX, United States, 1 510(k) clearance
The University of Texas MD Anderson Cancer Center, Department of Radiation Physics, Division of Radiation Oncology is registered with the FDA (registration 3030564015) in Houston, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 17, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3030564015
- Address
- 1515 Holcombe Blvd., Houston, TX, United States, 77030
- Owner or operator
- The University of Texas MD Anderson Cancer Center (10090229)
- Roles
- Manufacturer
- First device listed
- February 29, 2024
- Registered through
- 2026
- Brand names listed
- Radiation Planning Assistant
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Planning, Radiation Therapy Treatment | MUJ | 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 |
|---|---|---|---|---|---|---|
| May 17, 2023 | K222728 | Radiation Planning Assistant (RPA) | MUJ | Substantially Equivalent | University of Texas, MD Anderson Cancer Center | accessdata.fda.gov |
Compare with other makers
Updated May 17, 2023. 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.