Sonora Respiratory Products, Inc.
Country not established
- Devices
- 1
What Sonora Respiratory Products, Inc. makes
Sonora Respiratory Products, Inc. manufactures the MISTMASTER, a nebulizer designed for delivering respiratory medications in aerosol form to patients.
The MISTMASTER is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Mistmaster Ref K872315
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonora Respiratory Products, Inc. have in the registry?
The registry currently lists 1 device for Sonora Respiratory Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonora Respiratory Products, Inc.'s devices?
Among its 1 most recently registered device, Sonora Respiratory Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sonora Respiratory Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sonora Respiratory Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sonora Respiratory Products, Inc. in the registry?
The most recently registered devices listed for Sonora Respiratory Products, Inc. include MISTMASTER.