Resitu Medical AB
SwedenFDA applicant, unverified FDA FEI 3044399745
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Resitu Medical AB makes
Resitu Medical AB makes the Resitu Slider 09 (RESL09), a medical device designed for specific clinical use.
The Resitu Slider 09 (RESL09) is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Resitu Slider 09 (RESL09) Ref K252183
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3044399745
- Address
- Rapsgatan 7A, Uppsala
Frequently asked questions
How many devices does Resitu Medical AB have in the registry?
The registry currently lists 1 device for Resitu Medical AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Resitu Medical AB's devices?
Among its 1 most recently registered device, Resitu Medical AB has devices listed in FDA 510(k) (1 device).
What risk classes do Resitu Medical AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Resitu Medical AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Resitu Medical AB in the registry?
The most recently registered devices listed for Resitu Medical AB include Resitu Slider 09 (RESL09).