Dermatron Corp.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Uva Phototherapy System Ref K761094
Regimes: 510(k) Registry: 510(k)Black Lamps, F72T12/Bl/Ho Ref K770862
Regimes: 510(k) Registry: 510(k)Lamp, Flourescent Black, High Output Ref K760471
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Sunlamp (F40-Uvb & F20-Uvb) Ref K760482
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermatron Corp. have in the registry?
The registry currently lists 5 devices for Dermatron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermatron Corp.'s devices?
Among its 5 most recently registered devices, Dermatron Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Dermatron Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Dermatron Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermatron Corp. in the registry?
The most recently registered devices listed for Dermatron Corp. include UVA PHOTOTHERAPY SYSTEM, BLACK LAMPS, F72T12/BL/HO, LAMP, FLOURESCENT BLACK, HIGH OUTPUT and SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313.