Data / Medical devices / United States / Diacor, Inc.
Diacor, Inc.: FDA-registered device maker in Mount Pleasant, UT, United States, 1 510(k) clearance
Diacor, Inc. is registered with the FDA (registration 1721113) in Mount Pleasant, UT, United States. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 17, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1721113
- Address
- 1236 South Airstrip Lane, Mount Pleasant, UT, United States, 84647
- Owner or operator
- DIACOR, INC. (1721113)
- Roles
- Manufacturer
- First device listed
- May 18, 2009
- Registered through
- 2026
- Brand names listed
- Blower Accessories (ZBL-2MR), Diacor Carbon Fiber GE CT Overlay, Diacor Carbon Fiber GE CT Overlay with Stops, Diacor Carbon Fiber Toshiba CT Overlay, Diacor GE GEM Cart Overlay, Diacor GE GEM Cart Overlay 2-piece, Diacor Kevlar GE PET/MR Overlay, Diacor Wheeled Stretcher and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accelerator, Linear, Medical | IYE | 2 | Manufacturer | accessdata.fda.gov |
| Device, Patient Transfer, Powered | FRZ | 2 | Manufacturer | accessdata.fda.gov |
| Stretcher, Wheeled | FPO | 2 | Manufacturer | accessdata.fda.gov |
| System, Nuclear Magnetic Resonance Imaging | LNH | 2 | Manufacturer | accessdata.fda.gov |
| System, Radiation Therapy, Charged-Particle, Medical | LHN | 2 | Manufacturer | accessdata.fda.gov |
| Table, Radiographic, Stationary Top | IXQ | 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 |
|---|---|---|---|---|---|---|
| January 17, 2013 | K121929 | ZEPHYR 'X-SERIES PATIENT TRANSFER SLED | FRZ | Substantially Equivalent | Diacor, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Patient Transfer, Powered
- All makers of System, Radiation Therapy, Charged-Particle, Medical
- All makers of Accelerator, Linear, Medical
- All makers of System, Nuclear Magnetic Resonance Imaging
- All makers of Stretcher, Wheeled
- All makers of Table, Radiographic, Stationary Top
Updated January 17, 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.