Pulsonic Ag, Medical Technology is one of 23674 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulsonic Ag, Medical Technology - FDA 510(k) Cleared Devices
Recent clearances: CARDIOSCOPE SONOPLUS 3000
1
Total
1
Cleared
0
Denied
Pulsonic Ag, Medical Technology has 1 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pulsonic Ag, Medical Technology 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 - Pulsonic Ag, Medical Technology
1 devices