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.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Airstrip Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5