American Urologicals, Inc.
Country not established
- Devices
- 1
What American Urologicals, Inc. makes
American Urologicals, Inc. manufactures a resectoscope with an electrocautery cutting loop, designed for transurethral resection procedures in urological surgery.
The company’s products are regulated as Class II medical devices in the US and are listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Resectoscope Electro Cautery Cutting Loop Ref K943879
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Urologicals, Inc. have in the registry?
The registry currently lists 1 device for American Urologicals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Urologicals, Inc.'s devices?
Among its 1 most recently registered device, American Urologicals, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do American Urologicals, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Urologicals, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Urologicals, Inc. in the registry?
The most recently registered devices listed for American Urologicals, Inc. include RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP.