Data / Medical devices / United States / Radiological Imaging Technology, Inc.
Radiological Imaging Technology, Inc.: FDA-registered device maker in Co Spgs, CO, United States, 1 510(k) clearance
Radiological Imaging Technology, Inc. is registered with the FDA (registration 1722661) in Co Spgs, CO, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 29, 1994. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 1722661
- FEI number
- 1000160359
- Address
- 5065 List Drive, Co Spgs, CO, United States, 80919
- Owner or operator
- RADIOLOGICAL IMAGING TECHNOLOGY, INC. (9009383)
- Roles
- Manufacturer
- First device listed
- February 1, 1994
- Registered through
- 2026
- Brand names listed
- RIT Classic, RIT Complete, RIT Complete Diagnostic, RIT EPID MLC, RIT EPID MLC with Isocenter, RIT Family of Products, RIT Film, RIT Isocenter Analysis Tool and more
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 |
|---|---|---|---|---|---|---|
| July 29, 1994 | K935928 | RIT 113 FILM ANALYSIS SYSTEM | IYE | Substantially Equivalent | Radiological Imaging Technology, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 29, 1994. 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.