A. B. Vacuum Extractor, Inc.
Country not established
- Devices
- 1
What A. B. Vacuum Extractor, Inc. makes
A. B. Vacuum Extractor, Inc. manufactures the HYSTEROSER, a medical device designed for vacuum extraction procedures.
The HYSTEROSER is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Hysteroser Ref K791330
510(k) 510(k)
Frequently asked questions
How many devices does A. B. Vacuum Extractor, Inc. have in the registry?
The registry currently lists 1 device for A. B. Vacuum Extractor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list A. B. Vacuum Extractor, Inc.'s devices?
Among its 1 most recently registered device, A. B. Vacuum Extractor, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do A. B. Vacuum Extractor, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for A. B. Vacuum Extractor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A. B. Vacuum Extractor, Inc. in the registry?
The most recently registered devices listed for A. B. Vacuum Extractor, Inc. include HYSTEROSER.