Palaistra Systems, Inc. is one of 24136 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Palaistra Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: THE HERMES SYSTEM
1
Total
1
Cleared
0
Denied
Palaistra Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Palaistra Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Palaistra Systems, Inc.
1 devices