Radi Medical Systems AB
Radi Medical Systems AB holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2013.
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.