Betta Medical, Inc.
Country not established
- Devices
- 1
What Betta Medical, Inc. makes
Betta Medical, Inc. manufactures fine-needle aspiration (FNA) biopsy needles, designed for diagnostic sampling of soft tissues and lesions.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Fna Biopsy Needle Ref K941722
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Betta Medical, Inc. have in the registry?
The registry currently lists 1 device for Betta Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Betta Medical, Inc.'s devices?
Among its 1 most recently registered device, Betta Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Betta Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Betta Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Betta Medical, Inc. in the registry?
The most recently registered devices listed for Betta Medical, Inc. include FNA BIOPSY NEEDLE.