Rowheels, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rowheels, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rowheels Revolution 1.0
1
Total
1
Cleared
0
Denied
Rowheels, Inc. has 1 FDA 510(k) cleared medical devices. Based in Middleton, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Rowheels, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by FDA Compliance Group as regulatory consultant.
FDA 510(k) Regulatory Record - Rowheels, Inc.
1 devices