Pleural Dynamics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pleural Dynamics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Automatic Continuous Effusion Shunt (ACES) System ACES System
1
Total
1
Cleared
0
Denied
Pleural Dynamics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Wayzata, US.
Last cleared in 2023. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pleural Dynamics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ostendorf Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pleural Dynamics, Inc.
1 devices