Palo Alto Health Sciences, Inc. is one of 5511 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
Recent clearances: Freespira
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.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Palo Alto Health Sciences, Inc.
2 devices