RadScan Medical Equipment, Inc.
United Statesfrom the FDA registration address FDA FEI 3004185485
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Radscan Equipment Slicker Ref K101350
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004185485
- Address
- 23910 N 19th Ave Ste B4-66, PHOENIX, AZ, 85085
- Website
- radscanmedical.com/
From the company website
For over 30 years RadScan Medical Equipment has been a market-leading medical device accessory company that develops and manufactures a wide range of high quality products and accessories for various medical devices that help you safeguard and maintain your sensitive medical equipment as well as prioritizing the safety of your staff and patients.
Frequently asked questions
How many devices does RadScan Medical Equipment, Inc. have in the registry?
The registry currently lists 1 device for RadScan Medical Equipment, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list RadScan Medical Equipment, Inc.'s devices?
Among its 1 most recently registered device, RadScan Medical Equipment, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do RadScan Medical Equipment, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for RadScan Medical Equipment, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from RadScan Medical Equipment, Inc. in the registry?
The most recently registered devices listed for RadScan Medical Equipment, Inc. include RADSCAN EQUIPMENT SLICKER.