Wavepulse (Xiamen) Healthcare Technology Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Air Compression Massager (EP30B001 I) Ref K260948
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wavepulse (Xiamen) Healthcare Technology Co., Ltd. have in the registry?
The registry currently lists 1 device for Wavepulse (Xiamen) Healthcare Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wavepulse (Xiamen) Healthcare Technology Co., Ltd.'s devices?
Among its 1 most recently registered device, Wavepulse (Xiamen) Healthcare Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Wavepulse (Xiamen) Healthcare Technology Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wavepulse (Xiamen) Healthcare Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wavepulse (Xiamen) Healthcare Technology Co., Ltd. in the registry?
The most recently registered devices listed for Wavepulse (Xiamen) Healthcare Technology Co., Ltd. include Air Compression Massager (EP30B001 I).