Scarlet Rf, Inc.
Country not established
- Devices
- 1
What Scarlet Rf, Inc. makes
Scarlet Rf, Inc. makes the Hyperion Long Pulsed Nd:YAG Laser, a medical laser device used for dermatological and aesthetic procedures.
The Hyperion Long Pulsed Nd:YAG Laser is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Hyperion Long Pulsed Nd: Yag Laser Ref K132286
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scarlet Rf, Inc. have in the registry?
The registry currently lists 1 device for Scarlet Rf, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scarlet Rf, Inc.'s devices?
Among its 1 most recently registered device, Scarlet Rf, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Scarlet Rf, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Scarlet Rf, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scarlet Rf, Inc. in the registry?
The most recently registered devices listed for Scarlet Rf, Inc. include HYPERION LONG PULSED ND: YAG LASER.