Medical Device Manufacturer · US , Vista , CA

Aperio Technologies - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

Aperio Technologies has 5 FDA 510(k) cleared medical devices. Based in Vista, US.

Historical record: 5 cleared submissions from 2007 to 2009. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by Aperio Technologies Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Aperio Technologies

5 devices

1-5 of 5