Idaho Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Idaho Technology, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Idaho Technology, Inc. has 8 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 8 cleared submissions from 2005 to 2012. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Idaho Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Idaho Technology, Inc.
8 devices
Cleared
May 15, 2012
FILMARRAY RP PANEL
Microbiology
106d
Cleared
May 20, 2011
JBAIDS Q FEVER DETECTION KIT
Microbiology
200d
Cleared
Apr 27, 2011
FILMARRAY RP PANEL
Microbiology
40d
Cleared
Feb 17, 2011
FILMARRAY RESPIRATORY PANEL (RP)
Microbiology
112d
Cleared
Dec 20, 2007
JBAIDS PLAQUE DETECTION KIT, MODEL JRPD-ASY-0123
Microbiology
93d
Cleared
Dec 19, 2007
JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124
Microbiology
100d
Cleared
May 21, 2007
MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM
Microbiology
21d
Cleared
Nov 18, 2005
JBAIDS ANTHRAC DETECTION SYSTEM
Microbiology
144d