Phoenix Medical Devices, LLC is one of 24201 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phoenix Medical Devices, LLC - FDA 510(k) Cleared Devices
Recent clearances: PMD-2000 INTERFERENTIAL STIMULATOR
1
Total
1
Cleared
0
Denied
Phoenix Medical Devices, LLC has 1 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Phoenix Medical Devices, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Phoenix Medical Devices, LLC
1 devices