Airstrip Technologies, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
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) cleared devices by Airstrip Technologies, Inc.
5 devices
Cleared
Dec 09, 2021
AirStrip ONE Web Client with Alarm Communication Management (ACM)
Cardiovascular
169d
Cleared
Sep 11, 2018
AirStrip RPM InvisionHeart Adapter
Cardiovascular
26d
Cleared
Sep 19, 2016
AirStrip RPM
Cardiovascular
174d
Cleared
Mar 10, 2015
Sense4Baby System Model B+ (MSA)
Obstetrics & Gynecology
131d
Cleared
Nov 20, 2012
AIRSTRIP RPM FOR LIFENET CONSULT
Cardiovascular
162d