Data / Medical devices / United States / Radscan Medical Equipment, Inc.
Radscan Medical Equipment, Inc.: FDA-registered device maker in Phoenix, AZ, United States, 1 510(k) clearance
Radscan Medical Equipment, Inc. is registered with the FDA (registration 2032841) in Phoenix, AZ, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 4, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2032841
- FEI number
- 3004185485
- Address
- 23910 N 19th Ave Ste B4-66, Phoenix, AZ, United States, 85085
- Owner or operator
- RADSCAN MEDICAL EQUIPMENT, INC. (9059066)
- Roles
- Manufacturer, Specification developer
- First device listed
- December 6, 2011
- Registered through
- 2026
- Brand names listed
- CT Slicker Cushion, RadScan Equipment Slicker, RadScan Slicker Covers, Slicker Foot Switch/Machine Protective Covers
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cover, Mattress (Medical Purposes) | FMW | 1 | Manufacturer | accessdata.fda.gov |
| Curtain, Protective, Radiographic | IWQ | 1 | Manufacturer | accessdata.fda.gov |
| Drape, Surgical, Antimicrobial | KKX | 2 | Specification developer | accessdata.fda.gov |
| Support, Patient Position | CCX | 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 |
|---|---|---|---|---|---|---|
| January 4, 2011 | K101350 | RADSCAN EQUIPMENT SLICKER | KKX | Substantially Equivalent | Radscan Medical Equipment, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Support, Patient Position
- All makers of Curtain, Protective, Radiographic
- All makers of Cover, Mattress (Medical Purposes)
- All makers of Drape, Surgical, Antimicrobial
Updated January 4, 2011. 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.