American Biomed, Inc.
Country not established
- Devices
- 1
What American Biomed, Inc. makes
American Biomed, Inc. manufactures a single lumen embolectomy catheter, designed for the removal of thromboembolic material from blood vessels.
The company’s products are regulated as Class II devices under FDA 510(k) clearance and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Single Lumen Embolectomy Catheter Ref K972572
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Biomed, Inc. have in the registry?
The registry currently lists 1 device for American Biomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Biomed, Inc.'s devices?
Among its 1 most recently registered device, American Biomed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do American Biomed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Biomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Biomed, Inc. in the registry?
The most recently registered devices listed for American Biomed, Inc. include SINGLE LUMEN EMBOLECTOMY CATHETER.