Deep Breathe, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Deep Breathe, Inc. makes
Deep Breathe, Inc. manufactures the BlineSlide, a medical device designed for respiratory therapy, likely intended to assist with airway management or ventilation support in clinical settings.
The BlineSlide is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
BlineSlide Ref K252007
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deep Breathe, Inc. have in the registry?
The registry currently lists 1 device for Deep Breathe, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deep Breathe, Inc.'s devices?
Among its 1 most recently registered device, Deep Breathe, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Deep Breathe, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Deep Breathe, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deep Breathe, Inc. in the registry?
The most recently registered devices listed for Deep Breathe, Inc. include BlineSlide.