FDA 510(k) Applications Submitted by MATS GRANLUND

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980898	03/09/1998	FEMOSTOP II DISPOSABLE SET, FEMOSTOP II COMPRESSION ARCH, FEMOSTOP II PUMP, FEMOSTOP II BILATERAL ADAPTER	RADI MEDICAL SYSTEMS AB
K031662	05/28/2003	PRESSURE WIRE SENSOR, MODELS 12004/12304	RADI MEDICAL SYSTEMS AB
K982182	06/22/1998	FEMOSTOP II PLUS DISPOSABLE SET MODEL 11166, FEMOSTOP II PLUS COMPRESSION ARCH MODEL 11168, FEMOSTOP II BILATERAL ADAPT0	RADI MEDICAL SYSTEMS AB
K022187	07/05/2002	PRESSURE WIRE SENSOR, MODELS 12003/12303, 12004/12304	RADI MEDICAL SYSTEMS AB
K022188	07/05/2002	RADIANALYZER, MODEL 12710	RADI MEDICAL SYSTEMS AB
K002067	07/07/2000	RADIANALYZER, MODEL 12710	RADI MEDICAL SYSTEMS AB
K092105	07/14/2009	RADIANALYZER XPRESS	RADI MEDICAL SYSTEMS AB
K972793	07/28/1997	PRESSURE WIRE SENSOR .014, PRESSURE WIRE INTERFACE 10, PRESSURE WIRE MONITOR CABLE	RADI MEDICAL SYSTEMS AB
K062769	09/15/2006	PRESSUREWIRE CERTUS, MODELS 12006 AND 12306	RADI MEDICAL SYSTEMS AB
K002962	09/22/2000	PRESSURE WIRE SENSOR, MODEL 12003/12303	RADI MEDICAL SYSTEMS AB
K983471	10/02/1998	FEMOSTOP COMPRESSION ARCH, FEMOSTOP PUMP, FEMOSTOP BILATERAL ADAPTER	RADI MEDICAL SYSTEMS AB
K983506	10/07/1998	PRESSUREWIRE SENSOR, MODEL #12001	RADI MEDICAL SYSTEMS AB
K013943	11/29/2001	RADIANALYZER, MODEL 12710, RADIVIEW (PC-SOFTWARE ACCESSORY), MODEL 12720	RADI MEDICAL SYSTEMS AB
K024107	12/13/2002	FEMOSTOP FEMORAL COMPRESSION SYSTEM	RADI MEDICAL SYSTEMS AB