Multicept A/S
DenmarkFDA applicant, unverified
- Devices
- 1
What Multicept A/S makes
Multicept A/S manufactures the Multi Care Therapeutic Vibrator, a medical device designed for therapeutic vibration applications.
This product is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Multi Care Therapeutic Vibrator Ref K010096
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Multicept A/S have in the registry?
The registry currently lists 1 device for Multicept A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Multicept A/S's devices?
Among its 1 most recently registered device, Multicept A/S has devices listed in FDA 510(k) (1 device).
What risk classes do Multicept A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Multicept A/S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Multicept A/S in the registry?
The most recently registered devices listed for Multicept A/S include MULTI CARE THERAPEUTIC VIBRATOR.