Medical Device Marketing Network, Inc.
Country not established
- Devices
- 1
What Medical Device Marketing Network, Inc. makes
Medical Device Marketing Network, Inc. manufactures the Giotto Mammography HF, a high-frequency mammography system designed for breast imaging.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II device. The system is listed in the FDA’s 510(k) registry and the company is based in the United States.
Catalogue
Giotto Mammography Hf Ref K901558
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Device Marketing Network, Inc. have in the registry?
The registry currently lists 1 device for Medical Device Marketing Network, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Device Marketing Network, Inc.'s devices?
Among its 1 most recently registered device, Medical Device Marketing Network, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Device Marketing Network, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Device Marketing Network, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Device Marketing Network, Inc. in the registry?
The most recently registered devices listed for Medical Device Marketing Network, Inc. include GIOTTO MAMMOGRAPHY HF.