American Hair Removal System Co.
Country not established
- Devices
- 1
What American Hair Removal System Co. makes
American Hair Removal System Co. manufactures the AHRS EPILATOR 629, a Class I electrolysis device designed for professional hair removal through precise needle-based electrolysis technology.
The device is regulated under the FDA’s 510(k) pathway as a Class I medical device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Ahrs Epilator 629 Ref K892514
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Hair Removal System Co. have in the registry?
The registry currently lists 1 device for American Hair Removal System Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Hair Removal System Co.'s devices?
Among its 1 most recently registered device, American Hair Removal System Co. has devices listed in FDA 510(k) (1 device).
What risk classes do American Hair Removal System Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Hair Removal System Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from American Hair Removal System Co. in the registry?
The most recently registered devices listed for American Hair Removal System Co. include AHRS EPILATOR 629.