FDA 510(k) Application Details - K071188

Device Classification Name	More FDA Info for this Device
510(K) Number	K071188
Device Name	MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM
Applicant	IDAHO TECHNOLOGY, INC. 390 Wakara Way Salt Lake City, UT 84108 US Other 510(k) Applications for this Company
Contact	BETH LINGENFELTER Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	NHT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/30/2007
Decision Date	05/21/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review