Dermatology Assoc.
Country not established
- Devices
- 1
What Dermatology Assoc. makes
Dermatology Assoc. manufactures the ELCAT D-PPG, a plethysmography device designed for assessing blood flow and vascular responses in dermatological evaluations.
The company’s portfolio is regulated under FDA’s Class II device classification, with the ELCAT D-PPG listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Elcat D-Ppg, Plethysmograph Device Ref K944395
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermatology Assoc. have in the registry?
The registry currently lists 1 device for Dermatology Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermatology Assoc.'s devices?
Among its 1 most recently registered device, Dermatology Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dermatology Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermatology Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermatology Assoc. in the registry?
The most recently registered devices listed for Dermatology Assoc. include ELCAT D-PPG, PLETHYSMOGRAPH DEVICE.