Patient Pocket, LLC is one of 18397 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Patient Pocket, LLC - FDA 510(k) Cleared Devices
Recent clearances: LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDock, Laser Dock
2
Total
2
Cleared
0
Denied
Patient Pocket, LLC has 2 FDA 510(k) cleared medical devices. Based in Cherry Hill, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Patient Pocket, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Licensale, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Patient Pocket, LLC
2 devices