Medical Device Manufacturer · US , San Antonio , TX

Airstrip Technologies, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

Total

Cleared

Denied

Airstrip Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Antonio, US.

Last cleared in 2021. Active since 2012. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Airstrip Technologies, Inc.

5 devices

1-5 of 5