Ryan Telemedicine is one of 25741 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ryan Telemedicine - FDA 510(k) Cleared Devices
Recent clearances: INTERFERENTIAL STIMULATOR, MODEL NETWAVE, INTERFERENTIAL STIMULATOR, MODEL RTM1000
2
Total
2
Cleared
0
Denied
Ryan Telemedicine has 2 FDA 510(k) cleared medical devices. Based in Costa Mesa, US.
Historical record: 2 cleared submissions from 2003 to 2003. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Ryan Telemedicine Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Intertek Testing Services.
FDA 510(k) Regulatory Record - Ryan Telemedicine
2 devices