Murray, Salk, Inc.
Country not established
- Devices
- 1
What Murray, Salk, Inc. makes
Murray, Salk, Inc. manufactures AQUA-GEL, a wound care hydrogel designed for moist wound healing and debridement support.
The company’s product portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The company is based in the US.
Catalogue
Aqua-Gel Ref K781032
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Murray, Salk, Inc. have in the registry?
The registry currently lists 1 device for Murray, Salk, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Murray, Salk, Inc.'s devices?
Among its 1 most recently registered device, Murray, Salk, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Murray, Salk, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Murray, Salk, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Murray, Salk, Inc. in the registry?
The most recently registered devices listed for Murray, Salk, Inc. include AQUA-GEL.