Power Medical Devices, LLC is one of 21396 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Power Medical Devices, LLC - FDA 510(k) Cleared Devices
Recent clearances: Pacifier Activated Lullaby (PAL®)
1
Total
1
Cleared
0
Denied
Power Medical Devices, LLC has 1 FDA 510(k) cleared medical devices. Based in Delray Beach, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Power Medical Devices, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Power Medical Devices, LLC
1 devices