Precision Professional Products
Country not established
- Devices
- 1
What Precision Professional Products makes
Precision Professional Products manufactures the P.P.P. Treatment Cabinet, a device designed for localized therapeutic treatments, likely used in professional or clinical settings for procedures such as UV light therapy or ozone treatment.
The company’s portfolio is regulated under FDA Class I devices and requires 510(k) clearance. The manufacturer is based in the United States.
Catalogue
P.P.P. Treatment Cabinet Ref K813003
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Professional Products have in the registry?
The registry currently lists 1 device for Precision Professional Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Professional Products's devices?
Among its 1 most recently registered device, Precision Professional Products has devices listed in FDA 510(k) (1 device).
What risk classes do Precision Professional Products's devices fall under?
Among its 1 most recently registered device, the classes recorded for Precision Professional Products's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Precision Professional Products in the registry?
The most recently registered devices listed for Precision Professional Products include P.P.P. TREATMENT CABINET.