Et Medical Devices Spa
ItalyFDA 510(k) applicant, unverified
- Devices
- 3
What Et Medical Devices Spa makes
Et Medical Devices Spa manufactures the WALK400H, a gait analysis and rehabilitation device, as well as the CARDIOLINE series (AR 600, AR 1200, AR 2100) for cardiac monitoring and rehabilitation, and the CARDITTE MICROTEL, a portable cardiac monitoring system.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
WALK400H Ref K091054
510(k) 510(k)Cardioline Ar 600, Ar 1200, Ar 2100 Ref K051534
510(k) 510(k)Carditte Microtel Ref K082124
510(k) 510(k)
Frequently asked questions
How many devices does Et Medical Devices Spa have in the registry?
The registry currently lists 3 devices for Et Medical Devices Spa. Devices recorded under merged duplicate company entries are counted once.
Which registries list Et Medical Devices Spa's devices?
Among its 3 most recently registered devices, Et Medical Devices Spa has devices listed in FDA 510(k) (3 devices).
What risk classes do Et Medical Devices Spa's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Et Medical Devices Spa's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Et Medical Devices Spa in the registry?
The most recently registered devices listed for Et Medical Devices Spa include WALK400H, CARDIOLINE AR 600, AR 1200, AR 2100 and CARDITTE MICROTEL.