Aperio Services, LLC is one of 25221 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aperio Services, LLC - FDA 510(k) Cleared Devices
Recent clearances: NEWTOM 3G QR-DVT 9000, NEWTOM QR-DVT 9000
2
Total
2
Cleared
0
Denied
Aperio Services, LLC has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 2001 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aperio Services, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aperio Services, LLC
2 devices