ClearanceBrief
Company ยท US

Idaho Technology, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2012. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NHTAssay, Nucleic Acid Amplification, Bacillus Anthracis3
OCCRespiratory Virus Panel Nucleic Acid Assay System3
OEHJoint Biological Agent Identification And Diagnostic System (Jbaids) Tularemia Detection Kit1
OVFAssay, Direct, Nucleic Acid Amplification, Q Fever1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 15, 2012K120267FILMARRAY RP PANEL
Idaho Technology, Inc.
OCC
May 20, 2011K103207JBAIDS Q FEVER DETECTION KIT
Idaho Technology, Inc.
OVF
Apr 27, 2011K110764FILMARRAY RP PANEL
Idaho Technology, Inc.
OCC
Feb 17, 2011K103175FILMARRAY RESPIRATORY PANEL (RP)
Idaho Technology, Inc.
OCC
Dec 20, 2007K072631JBAIDS PLAQUE DETECTION KIT, MODEL JRPD-ASY-0123
Idaho Technology, Inc.
NHT
Dec 19, 2007K072547JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124
Idaho Technology, Inc.
OEH
May 21, 2007K071188MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM
Idaho Technology, Inc.
NHT
Nov 18, 2005K051713JBAIDS ANTHRAC DETECTION SYSTEM
Idaho Technology, Inc.
NHT

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes