Rivertrail Mobility is one of 25088 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Rivertrail Mobility has 1 FDA 510(k) cleared medical devices. Based in Clinton, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Rivertrail Mobility 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 - Rivertrail Mobility
1 devices