FDA 510(k) Application Details - K132251

Device Classification Name	Dna-Reagents, Neisseria   More FDA Info for this Device
510(K) Number	K132251
Device Name	Dna-Reagents, Neisseria
Applicant	HOLOGIC / GEN-PROBE INCORPORATED 10210 GENETIC CENTER DRIVE SAN DIEGO, CA 92121-4376 US Other 510(k) Applications for this Company
Regulation Number	866.3390   More FDA Info for this Regulation Number
Classification Product Code	LSL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/19/2013
Decision Date	10/17/2013
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