Palo Alto Health Sciences, Inc. is one of 5146 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Palo Alto Health Sciences, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Palo Alto Health Sciences, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 2 cleared submissions from 2013 to 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Palo Alto Health Sciences, Inc. Filter by specialty or product code using the sidebar.
Palo Alto Health Sciences, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Aug 23, 2018
Freespira
Neurology
213d
Cleared
Dec 10, 2013
CANARY BREATHING SYSTEM
Neurology
193d