Anacom General Corp.
Country not established
- Devices
- 1
What Anacom General Corp. makes
Anacom General Corp. manufactures the DERMATEK 4000, a device designed for dermatological imaging and analysis, likely used in skin condition assessment or diagnostic procedures.
The DERMATEK 4000 is classified as a Class II medical device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Dermatek 4000 Ref K911057
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anacom General Corp. have in the registry?
The registry currently lists 1 device for Anacom General Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anacom General Corp.'s devices?
Among its 1 most recently registered device, Anacom General Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Anacom General Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Anacom General Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anacom General Corp. in the registry?
The most recently registered devices listed for Anacom General Corp. include DERMATEK 4000.