Skylark Device & Systems Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Bio-Stim Kit Ref K050174
Regimes: 510(k) Registry: 510(k)Sds-4I Ref K034005
Regimes: 510(k) Registry: 510(k)Conductive Gel For Ultrasound Ref K002832
Regimes: 510(k) Registry: 510(k)Sd-730 If-Sds, Perfect Pulse If-Sds Ref K992652
Regimes: 510(k) Registry: 510(k)Skylark Uro Probe Ref K053007
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Skylark Device & Systems Co., Ltd. have in the registry?
The registry currently lists 6 devices for Skylark Device & Systems Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Skylark Device & Systems Co., Ltd.'s devices?
Among its 6 most recently registered devices, Skylark Device & Systems Co., Ltd. has devices listed in FDA 510(k) (6 devices).
What risk classes do Skylark Device & Systems Co., Ltd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Skylark Device & Systems Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Skylark Device & Systems Co., Ltd. in the registry?
The most recently registered devices listed for Skylark Device & Systems Co., Ltd. include SKYLARK INFRARED PHOTON STIMULATOR, MODELS, SD-956IR AND SD-100IR, BIO-STIM KIT, SDS-4I and CONDUCTIVE GEL FOR ULTRASOUND.