Medical Device Manufacturer · US , Fort Myers , FL

Pulsaderm, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

Pulsaderm, LLC has 3 FDA 510(k) cleared medical devices. Based in Fort Myers, US.

Historical record: 3 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Pulsaderm, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Pulsaderm, LLC

3 devices

1-3 of 3