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
K954669 10/10/1995 FEMOSTOP, FEMOSTOP PUMP 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


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