FDA 510(k) Application Details - K954923

Device Classification Name	Monitor, Microbial Growth   More FDA Info for this Device
510(K) Number	K954923
Device Name	Monitor, Microbial Growth
Applicant	BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS 7 LOVETON CIRCLE SPARKS, MD 21152-0999 US Other 510(k) Applications for this Company
Contact	DAVID R MERTZ Other 510(k) Applications for this Contact
Regulation Number	866.2560   More FDA Info for this Regulation Number
Classification Product Code	JTA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/26/1995
Decision Date	11/21/1996
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