Intermed Group, Inc.
Country not established
- Devices
- 1
What Intermed Group, Inc. makes
Intermed Group, Inc. manufactures the INTERMED ZOOM COLPOSCOPE, which is a medical device used for gynecological examinations.
The INTERMED ZOOM COLPOSCOPE is classified as a Class II device and is listed in the FDA 510(k) registry. Intermed Group, Inc. is based in the US.
Catalogue
Intermed Zoom Colposcope Ref K031639
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intermed Group, Inc. have in the registry?
The registry currently lists 1 device for Intermed Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intermed Group, Inc.'s devices?
Among its 1 most recently registered device, Intermed Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intermed Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intermed Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intermed Group, Inc. in the registry?
The most recently registered devices listed for Intermed Group, Inc. include INTERMED ZOOM COLPOSCOPE.