Psoralite Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Psoralite Corp. makes
Psoralite Corp. manufactures phototherapy treatment equipment, including the PSORALITE PHOTOTHERAPY TREATMENT BOOTH MDL 45000, PSORALITE 18400 SERIES, PSORALITE 12800 SERIES, and PSORALITE PHOTOTHERAPY TREATMENT BOOTH/PANEL.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. Psoralite Corp. is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Psoralite 18400 Series Ref K864511
Regimes: 510(k) Registry: 510(k)Psoralite 12800 Series Ref K864510
Regimes: 510(k) Registry: 510(k)Psoralite, Phototherapy Treatment Equipment Ref K913760
Regimes: 510(k) Registry: 510(k)Psoralite Phototherapy Treatment Booth/Panel Ref K881385
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Psoralite Corp. have in the registry?
The registry currently lists 5 devices for Psoralite Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Psoralite Corp.'s devices?
Among its 5 most recently registered devices, Psoralite Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Psoralite Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Psoralite Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Psoralite Corp. in the registry?
The most recently registered devices listed for Psoralite Corp. include PSORALITE PHOTOTHERAPY TREATMENT BOOTH, MDL 45000, PSORALITE 18400 SERIES, PSORALITE 12800 SERIES and PSORALITE, PHOTOTHERAPY TREATMENT EQUIPMENT.