Palo Alto Health Sciences, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Palo Alto Health Sciences, Inc. makes
Palo Alto Health Sciences, Inc. manufactures the Canary Breathing System, a device designed for respiratory support and monitoring, and Freespira, a portable device for managing asthma and chronic obstructive pulmonary disease (COPD) symptoms through controlled breathing exercises.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are registered in the United States.
Catalogue
Canary Breathing System Ref K131586
Regimes: 510(k) Registry: 510(k)Freespira Ref K180173
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Palo Alto Health Sciences, Inc. have in the registry?
The registry currently lists 2 devices for Palo Alto Health Sciences, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Palo Alto Health Sciences, Inc.'s devices?
Among its 2 most recently registered devices, Palo Alto Health Sciences, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Palo Alto Health Sciences, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Palo Alto Health Sciences, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Palo Alto Health Sciences, Inc. in the registry?
The most recently registered devices listed for Palo Alto Health Sciences, Inc. include CANARY BREATHING SYSTEM and Freespira.