Radi Medical Systems AB
FDA 510(k) medical device clearances.
Top product codes for Radi Medical Systems AB
Recent clearances by Radi Medical Systems AB
- K123984 — QUANTIEN MEASUREMENT SYSTEM
- K092105 — RADIANALYZER XPRESS
- K080813 — PRESSUREWIRE CERTUS, CERTUS (300CM), AERIS, AERIS (300CM), RECEIVER
- K080206 — MODIFICATION TO FEMOSTOP FEMORAL COMPRESSION SYSTEM
- K062769 — PRESSUREWIRE CERTUS, MODELS 12006 AND 12306
- K042628 — MODIFICATION TO: RADIANALYZER, MODEL 12711
- K033291 — TOPSEAL HEMOSTATIC DRESSING, MODEL 11150
- K031662 — PRESSURE WIRE SENSOR, MODELS 12004/12304
- K024107 — FEMOSTOP FEMORAL COMPRESSION SYSTEM
- K022188 — RADIANALYZER, MODEL 12710
- K022187 — PRESSURE WIRE SENSOR, MODELS 12003/12303, 12004/12304
- K013943 — RADIANALYZER, MODEL 12710, RADIVIEW (PC-SOFTWARE ACCESSORY), MODEL 12720
- K002067 — RADIANALYZER, MODEL 12710
- K002962 — PRESSURE WIRE SENSOR, MODEL 12003/12303
- K983471 — FEMOSTOP COMPRESSION ARCH, FEMOSTOP PUMP, FEMOSTOP BILATERAL ADAPTER
- K983506 — PRESSUREWIRE SENSOR, MODEL #12001
- K982182 — FEMOSTOP II PLUS DISPOSABLE SET MODEL 11166, FEMOSTOP II PLUS COMPRESSION ARCH MODEL 11168, FEMOSTOP II BILATERAL ADAPT0
- K972793 — PRESSURE WIRE SENSOR .014, PRESSURE WIRE INTERFACE 10, PRESSURE WIRE MONITOR CABLE
- K980898 — FEMOSTOP II DISPOSABLE SET, FEMOSTOP II COMPRESSION ARCH, FEMOSTOP II PUMP, FEMOSTOP II BILATERAL ADAPTER
- K962425 — BONOPTY COAXIAL BONE BIOPSY SYSTEM WITH ECCENTRIC DRILL(10-1072,3,4)
- K954669 — FEMOSTOP, FEMOSTOP PUMP
- K944259 — FEMOSTOP II
- K915280 — FEMOSTOP
- K903622 — CT GUIDE (TM)
Data sourced from openFDA. This site is unofficial and independent of the FDA.