Pulmone Advanced Medical Devices, Ltd. is one of 5511 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
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.
FDA 510(k) Regulatory Record - Pulmone Advanced Medical Devices, Ltd.
3 devices