Mowbray Co., Inc.
Country not established
- Devices
- 1
What Mowbray Co., Inc. makes
Mowbray Co., Inc. manufactures DERMA PREP, a skin preparation solution used to reduce bacterial count on the skin prior to surgical procedures.
The company’s portfolio is regulated under Class I medical devices in the US, with devices listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Derma Prep Ref K851612
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mowbray Co., Inc. have in the registry?
The registry currently lists 1 device for Mowbray Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mowbray Co., Inc.'s devices?
Among its 1 most recently registered device, Mowbray Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mowbray Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mowbray Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mowbray Co., Inc. in the registry?
The most recently registered devices listed for Mowbray Co., Inc. include DERMA PREP.