D.E.A Project S.R.1.
ItalyFDA 510(k) applicant, unverified
- Devices
- 1
What D.E.A Project S.R.1. makes
D.E.A Project S.R.1. manufactures the Epildream HP 4000 MED, a medical device designed for laser hair removal procedures. This device uses advanced laser technology to target and reduce hair growth on the skin surface.
The Epildream HP 4000 MED is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Epildream HP 4000 MED Ref K222352
510(k) 510(k)
Frequently asked questions
How many devices does D.E.A Project S.R.1. have in the registry?
The registry currently lists 1 device for D.E.A Project S.R.1.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D.E.A Project S.R.1.'s devices?
Among its 1 most recently registered device, D.E.A Project S.R.1. has devices listed in FDA 510(k) (1 device).
What risk classes do D.E.A Project S.R.1.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for D.E.A Project S.R.1.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D.E.A Project S.R.1. in the registry?
The most recently registered devices listed for D.E.A Project S.R.1. include Epildream HP 4000 MED.