Urological, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cook Sidearm Core Tissue Biopsy Device Ref K041544
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Urological, Inc. have in the registry?
The registry currently lists 1 device for Urological, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Urological, Inc.'s devices?
Among its 1 most recently registered device, Urological, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Urological, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Urological, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Urological, Inc. in the registry?
The most recently registered devices listed for Urological, Inc. include COOK SIDEARM CORE TISSUE BIOPSY DEVICE.