Pulmone Advanced Medical Devices, Ltd. is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulmone Advanced Medical Devices, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MiniBox +, PULMONE MINIBOXPFT 2.0, PULMONE MINIBOX PFT TM
3
Total
3
Cleared
0
Denied
Pulmone Advanced Medical Devices, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Gaithersburg, US.
Historical record: 3 cleared submissions from 2014 to 2016. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Pulmone Advanced Medical Devices, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sfa Consulting, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Pulmone Advanced Medical Devices, Ltd.
3 devices