Jansson A/S
DenmarkFDA applicant, unverified
- Devices
- 1
What Jansson A/S makes
Jansson A/S manufactures the AKUFON Therapeutic Massager, a device designed for localized muscle and joint relief through mechanical vibration therapy.
The AKUFON Therapeutic Massager is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Akufon Therapeutic Massager Ref K850495
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jansson A/S have in the registry?
The registry currently lists 1 device for Jansson A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jansson A/S's devices?
Among its 1 most recently registered device, Jansson A/S has devices listed in FDA 510(k) (1 device).
What risk classes do Jansson A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jansson A/S's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jansson A/S in the registry?
The most recently registered devices listed for Jansson A/S include AKUFON THERAPEUTIC MASSAGER.