Revolutionary Medical Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Revolutionary Medical Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SuperNO2VA Et Device
2
Total
2
Cleared
0
Denied
Revolutionary Medical Devices, Inc. has 2 FDA 510(k) cleared medical devices. Based in Tucson, US.
Historical record: 2 cleared submissions from 2017 to 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Revolutionary Medical Devices, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedic, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Revolutionary Medical Devices, Inc.
2 devices