248 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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POSSIS ANGIOJET RAPID THROMBECTOMY CATHETER SYSTEM, F105 CATHETER,MODEL 3030C,LF140 CATHETER,MODEL 3040C,PUMP SET 3020P
FDA 510(k)
FDA Class 2
·Cardiovascular
TurboHawk Plus Directional Atherectomy System
FDA 510(k)
FDA Class 2
·Cardiovascular
FreedomFlow Orbital Circumferential Atherectomy System
FDA 510(k)
FDA Class 2
·Cardiovascular
Diamonback 360 Peripheral Orbital Atherectomy System, Diamondback 360 Stealth Orbital Atherectomy system
FDA 510(k)
FDA Class 2
·Cardiovascular
DIAMONDBACK 360 DEGREE ORBITAL ATHERECTOMY SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
CLEANER II ROTATIONAL THROMBECTOMY SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
ARROW-TREROTOLA PTD CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
THROMBOLYTIC BRUSH CATHETER, OVER THE WIRE (OTW)
FDA 510(k)
FDA Class 2
·Cardiovascular
Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy Catheters
FDA 510(k)
FDA Class 2
·Cardiovascular
JETSTREAM PATHWAY PC ATHERECTOMY SYSTEM, MODEL OV10300
FDA 510(k)
FDA Class 2
·Cardiovascular
JETSTREAM G3 (R) SF 1.6 SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
THERATEK GROUP EXCHANGE CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ORBITAL ATHERECTOMY SYSTEM FOR TREATMENT OF A-V SHUNT STENOSIS
FDA 510(k)
FDA Class 2
·Cardiovascular
Diamondback 360 Peripheral Orbital Atherectomy System
FDA 510(k)
FDA Class 2
·Cardiovascular
ViperWire Advance Guide Wire, Diamondback 360 Peripheral Orbital Atherectomy System, Stealth 360 Orbital PAD
FDA 510(k)
FDA Class 2
·Cardiovascular
SOLERA PLUS THROMBECTOMY CATHETER, 55 CM AND 110 CM, MODELS BAC SMG 007 055, BAC SMG 007 110
FDA 510(k)
FDA Class 2
·Cardiovascular
JETSTREAM G3 SE SYSTEM, JETSTREAM G3 SF SYSTEM MODEL PV31230 (JETSTREAM G3 SE CATHETER AND CONTROL POD); PVCN100 (PV CON
FDA 510(k)
FDA Class 2
·Cardiovascular
REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406
FDA 510(k)
FDA Class 2
·Cardiovascular
Pantheris System
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550, 04800, 05200, 06002, 02406, 04706, 04300,
FDA 510(k)
FDA Class 2
·Cardiovascular