Footdocprenur, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Footdocprenur, LLC - FDA 510(k) Cleared Devices
Recent clearances: REMY Medical Therapy Laser System
1
Total
1
Cleared
0
Denied
Footdocprenur, LLC has 1 FDA 510(k) cleared medical devices. Based in Cherry Hill, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Footdocprenur, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Braunsolutions as regulatory consultant.
FDA 510(k) Regulatory Record - Footdocprenur, LLC
1 devices