Advanced Instrument Development, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Advanced Instrument Development, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1979 to 1998. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Advanced Instrument Development, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Mar 17, 1998
IMIX DIGITAL THORAX SYSTEM
Radiology
78d
Cleared
Aug 12, 1987
POWER-AID INDEPENDENT X-RAY POWER SOURCE
Radiology
50d
Cleared
Jun 18, 1982
AUTOMATIC EXPOSURE CONTROL TYPE A3300
Radiology
28d
Cleared
Dec 03, 1981
MOBIL-AID AUTOMATIC EXPOSURE CONTROL
Radiology
28d
Cleared
Nov 13, 1979
CONVERSION CONTRACTOR TIMER KIT
Radiology
47d