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 |
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