FDA 510(k) Applications Submitted by JODY J FLEMING

FDA 510(k) Number	Submission Date	Device Name	Applicant
K111409	05/19/2011	APTIMA COMBO 2 ASSAY	GEN-PROBE, INC.
K981846	05/26/1998	PARENCHYMAL BOLT PRESSURE MONITORING KIT	CAMINO NEUROCARE, INC.
K982702	08/03/1998	VENTRIX SUBDURAL TUNNELING PRESSURE MONITORING KIT MODEL NL950-SD	CAMINO NEUROCARE, INC.