Aerotel Medical Systems (1998) , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aerotel Medical Systems (1998) , Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Aerotel Medical Systems (1998) , Ltd. has 7 FDA 510(k) cleared medical devices. Based in Hasbrouck Heights, US.
Historical record: 7 cleared submissions from 1999 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Aerotel Medical Systems (1998) , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aerotel Medical Systems (1998) , Ltd.
7 devices
Cleared
Oct 03, 2003
HEART 2006
Cardiovascular
29d
Cleared
Mar 28, 2003
MPM-NET
Cardiovascular
14d
Cleared
Nov 06, 2002
HEARTONE EVENT RECORDER AND TRANSMITTER
Cardiovascular
26d
Cleared
Jul 24, 2002
HEARTLINE RECEIVING STATION
Cardiovascular
28d
Cleared
May 22, 2002
TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM
Cardiovascular
16d
Cleared
May 17, 2000
HEART 2005
Cardiovascular
69d
Cleared
Sep 16, 1999
BP-TEL TRANS-TELEPHONIC BLOOD PRESSURE MEASUREMENT SYSTEM
Cardiovascular
330d