Hysterovue, Inc.
Country not established
- Devices
- 1
What Hysterovue, Inc. makes
Hysterovue, Inc. manufactures the Hystero-V Hysteroscope, a device used for visualizing the interior of the uterus during hysteroscopic procedures.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) premarket notification process. The company is based in the United States.
Catalogue
Hystero-V Hysteroscope Ref K202445
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hysterovue, Inc. have in the registry?
The registry currently lists 1 device for Hysterovue, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hysterovue, Inc.'s devices?
Among its 1 most recently registered device, Hysterovue, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hysterovue, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hysterovue, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hysterovue, Inc. in the registry?
The most recently registered devices listed for Hysterovue, Inc. include Hystero-V Hysteroscope.