Aqure Medical, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Anchor Dual Lumen Guidewire Catheter Ref K201076
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aqure Medical, Inc. have in the registry?
The registry currently lists 1 device for Aqure Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aqure Medical, Inc.'s devices?
Among its 1 most recently registered device, Aqure Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aqure Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aqure Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aqure Medical, Inc. in the registry?
The most recently registered devices listed for Aqure Medical, Inc. include Anchor Dual Lumen Guidewire Catheter.