Airstrip Technologies, LP is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Airstrip Technologies, LP - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Airstrip Technologies, LP has 10 FDA 510(k) cleared cardiovascular devices. Based in San Antonio, US.
Historical record: 10 cleared submissions from 2009 to 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
Airstrip Technologies, LP — FDA 510(k) Products and Clearance History
10 devices
Cleared
Feb 14, 2014
AIRSTRIP REMOTE PATIENT MONITORING
Cardiovascular
95d
Cleared
Feb 06, 2014
AIRSTRIP REMOTE PATIENT MONITORING
Cardiovascular
93d
Cleared
Jul 03, 2013
AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER
Cardiovascular
15d
Cleared
Oct 02, 2012
AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING
Cardiovascular
76d
Cleared
Jul 03, 2012
AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING
Cardiovascular
6d
Cleared
Aug 26, 2011
AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING
Cardiovascular
22d
Cleared
Mar 10, 2011
AIRSTRIP REMOTE PATIENT MONITORING (RPM)
Cardiovascular
16d
Cleared
Jul 23, 2010
AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE,...
Cardiovascular
185d
Cleared
Feb 13, 2009
AIRSTRIP OB
Obstetrics & Gynecology
10d
Cleared
Jan 23, 2009
AIRSTRIP OB
Obstetrics & Gynecology
14d