Deski
FranceFDA 510(k) applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Deski makes
Deski manufactures the HeartFocus device, a medical product designed for cardiac monitoring or intervention, as indicated by its name and versioning.
The HeartFocus device is classified under FDA Class II and is listed via the 510(k) pathway in the United States. The company is based in the US.
Catalogue
HeartFocus (V.1.1.1) Ref K242807
510(k) 510(k)
FDA establishments
- DESKi SAS Bordeaux Nouvelle-Aquitaine · FR FEI 3040362673
Frequently asked questions
How many devices does Deski have in the registry?
The registry currently lists 1 device for Deski. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deski's devices?
Among its 1 most recently registered device, Deski has devices listed in FDA 510(k) (1 device).
What risk classes do Deski's devices fall under?
Among its 1 most recently registered device, the classes recorded for Deski's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deski in the registry?
The most recently registered devices listed for Deski include HeartFocus (V.1.1.1).
Which FDA establishments are linked to Deski?
1 FDA establishment is linked to Deski in the registry; they are listed on the company page.