Medtronic Vascular
507 devices
Products
- Steerant Super Stiff GuidewireOtherFDA 510(k)
- 6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide CatheterOtherFDA 510(k)
- 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide CatheterOtherFDA 510(k)
- Heli-FX™ Ancillary EndoAnchor™ CassetteOtherFDA 510(k)
- 중심순환계색전제거용카테터OtherMFDS
- Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)OtherFDA 510(k)
- 중심순환계색전제거용카테터OtherMFDS
- Medtronic 6F Taiga Guiding CatheterOtherFDA 510(k)
- Heli-FX EndoAnchor SystemOtherFDA 510(k)
- Admiral XtremeOtherFDA 510(k)
- Sentrant Introducer Sheath with Hydrophilic CoatingOtherFDA 510(k)
- SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision SystemOtherFDA 510(k)
- Heli-FX Applier, Heli-FX Guide, Ancillary EndoAnchor CassetteOtherFDA 510(k)
- InTRAkitOtherFDA 510(k)
- TRAcelet Compression DeviceOtherFDA 510(k)
- HawkOne Directional Atherectomy SystemOtherFDA 510(k)
- DxTerity, DxTerity TRA, DxTerity Angio-Kit, DxTerity EZ-Pak, DxTerity TRA Angio-Kit, DxTerity TRA EZ-PakOtherFDA 510(k)
- TOTAL ACROSSOtherFDA 510(k)
- SENTRANT INTRODUCER SHEATH WITH HYDROPHILIC COATINGOtherFDA 510(k)
- PACIFIC PLUSOtherFDA 510(k)
- PIONEER PLUS CATHETER, MODEL PLUS 120OtherFDA 510(k)
- GTX GUIDEWIRE, MODELS TBD-GTX 1, 3,6,9,12, 15OtherFDA 510(k)
- 6F TAIGA GUIDING CATHETEROtherFDA 510(k)
- MEDTRONIC ANGIOGRAPHIC GUIDE WIRESOtherFDA 510(k)
- MEDTRONIC EXPORT AP CATHETEROtherFDA 510(k)
- COMPLETE SE SELF EXPANDING BILIARY STENT SYSTEMOtherFDA 510(k)
- AFFINITY PEDIATRIC ARTERIAL FILTER, MODEL S4014 AND WITH CARMEDA BIOACTIVE SURFACE, MODEL CB4014OtherFDA 510(k)
- CARDIOBLATE MONOPOLAR PEN, 60813, CARDIOBLATE MONOPOLAR XL, 60814OtherFDA 510(k)
- CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261Surgical InstrumentsFDA 510(k)
- SELECTSITE C304 DEFLECTABLE CATHETER SYSTEM, MODELS C304-S59, C304-L69, C304-XS59 & C304-XL74OtherFDA 510(k)
- CARDIOBLATE NAVIGATOR TISSUE DISSECTION DEVICEEndoscopyFDA 510(k)
- 5F SHERPA ACTIVE NX GUIDE CATHETEROtherFDA 510(k)
- MEDTRONIC EXPORT XT CATHETEROtherFDA 510(k)
- U-CLIP DEVICE, MODEL NC65OtherFDA 510(k)
- CG FUTURE ANNULOPLASTY SYSTEM, MODEL 638ROtherFDA 510(k)
- 8F SHERPA NX GUIDE CATHETEROtherFDA 510(k)
- 6248VAL ADJUSTABLE VALVEOtherFDA 510(k)
- MASTERGRAFT PUTTY BONE VOID FILLEROtherFDA 510(k)
- U-CLIP DEVICE, MODELS B140, B160 AND B180OtherFDA 510(k)
- TUNA SYSTEM, MODELS 8909, 8929, 8930, 8934Surgical InstrumentsFDA 510(k)
- 7F SHERPA NX GUIDE CATHETEROtherFDA 510(k)
- MODIFICATION TO: EXPORT CATHETEROtherFDA 510(k)
- CARDIOBLATE DISPERSIVE ELECTRODE ADAPTER (ACCESSORY), MODEL 60884Surgical InstrumentsFDA 510(k)
- 6F Z4 GUIDE CATHETEROtherFDA 510(k)
- HEPARIN DOSE RESPONSE CONTROLS, MODEL 306-20 POROtherFDA 510(k)
- HEPARINASE HR ACT CONTROL, MODEL 550-12OtherFDA 510(k)
- PURPLE/BLACK HEPARIN ASSAY CONTROLOtherFDA 510(k)
- HEPARIN DOSE RESPONSE CARTRIDGE, MODEL 304-20OtherFDA 510(k)
- ATTAIN SELECT 6238TEL GUIDE CATHETER SET FOR LEFT-HEART DELIVERYOtherFDA 510(k)
- MODEL 6416 TEMPORARY PACING LEAD SYSTEMOtherFDA 510(k)
- DETECT SURGICAL PACING AND MAPPING TOOLOtherFDA 510(k)
- POLYGRAM NET BIOFEEDBACK APPLICATIONOtherFDA 510(k)
- MEDTRONIC OCTOPUS TE STABILIZER & ACCESSORIESOtherFDA 510(k)
- EXPORT CATHETEROtherFDA 510(k)
- TRANSXCHANGE SUPPORT CATHETEROtherFDA 510(k)
- EN CIRCLR AL ADJUSTABLE LOOP MAPPING CATHETER MODELS, 1045AL1, 1045AL2, 1060AL1, 1060AL2OtherFDA 510(k)
- POLYETHER URETHANE MATERIAL CHANGE IN NEUROSTIMULATION LEADSOtherFDA 510(k)
- SPHERICAL TIP CORONARY OSTIAL CANNULA, MODEL 30011OtherFDA 510(k)
- ATTAIN 6226DEF DEFLECTABLE CATHETER DELIVERY SYSTEMOtherFDA 510(k)
- EKG SPEAKSOtherFDA 510(k)
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