FDA 510(k) Application Details - K051713

Device Classification Name	More FDA Info for this Device
510(K) Number	K051713
Device Name	JBAIDS ANTHRAC 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	06/27/2005
Decision Date	11/18/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review	Y