A&D Engineering, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A&D Engineering, Inc. - FDA 510(k) Cleared Devices
34
Total
34
Cleared
0
Denied
A&D Engineering, Inc. has 34 FDA 510(k) cleared cardiovascular devices. Based in San Jose, US.
Historical record: 34 cleared submissions from 1987 to 2008.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A&D Engineering, Inc.
34 devices
Cleared
Nov 13, 2008
A&D MEDICAL UA-851THW DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
56d
Cleared
Jan 19, 2007
A&D MEDICAL UA-789 DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
185d
Cleared
Jun 21, 2006
A & D MEDICAL UM-101 DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
27d
Cleared
Mar 03, 2005
A&D MEDICAL UA-767PBT DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
101d
Cleared
Dec 03, 2004
A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512
Cardiovascular
36d
Cleared
May 19, 2004
A & D MEDICAL UA-767BT DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
92d
Cleared
Mar 19, 2004
A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODEL UB-328
Cardiovascular
46d
Cleared
Oct 30, 2003
A & D MEDICAL LIFESOURCE UA-704 DIGITAL BLOOD PRESSURE MONITORS
Cardiovascular
78d
Cleared
Feb 15, 2002
A & D MEDICAL LIFESOURCE UA-781, UA781PC, & UA-781T DIGITAL BLOOD PRESSURE...
Cardiovascular
197d
Cleared
Jul 13, 2001
LIFESOURCE MODELS UA-787, UA 787PC, UA-787T
Cardiovascular
15d
Cleared
Mar 29, 2001
DIGITAL BLOOD PRESSURE MONITORS, MODELS TM-2655, TM-2655P, & TM-2655VP
Cardiovascular
9d
Cleared
Jan 19, 2001
A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR
Cardiovascular
197d