Medical Device Manufacturer · US , Sunnyvale , CA

Aptus Endosystems, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2011

Total

Cleared

Denied

Aptus Endosystems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 3 cleared submissions from 2011 to 2014. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Aptus Endosystems, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Aptus Endosystems, Inc.

4 devices

1-4 of 4