Wuhan Landing Medical Hi-Tech, Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Wuhan Landing Medical Hi-Tech, Ltd. makes
Wuhan Landing Medical Hi-Tech, Ltd. manufactures intermittent pneumatic compression devices, which are used to promote venous return and reduce the risk of deep vein thrombosis in patients.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance process. The manufacturer operates from the United States.
Catalogue
Intermittent Pneumatic Compression Device Ref K141390
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wuhan Landing Medical Hi-Tech, Ltd. have in the registry?
The registry currently lists 1 device for Wuhan Landing Medical Hi-Tech, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wuhan Landing Medical Hi-Tech, Ltd.'s devices?
Among its 1 most recently registered device, Wuhan Landing Medical Hi-Tech, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Wuhan Landing Medical Hi-Tech, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wuhan Landing Medical Hi-Tech, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wuhan Landing Medical Hi-Tech, Ltd. in the registry?
The most recently registered devices listed for Wuhan Landing Medical Hi-Tech, Ltd. include INTERMITTENT PNEUMATIC COMPRESSION DEVICE.