Thrombectomy Devices

May 27, 2014 — Ekos Corp. announced the U.S. Food and Drug Administration (FDA) has cleared the EkoSonic endovascular system for the ultrasound-facilitated, controlled and selective infusion of physician-specified fluids, including thrombolyt...

May 16, 2014 — In a move to expand significantly its portfolio of solutions for peripheral interventions, Boston Scientific Corp. has entered into a definitive agreement to acquire the interventional division of Bayer AG for $415 million...

Removing Blood Clots During PCI Does Not Improve Outcomes

According to a new study, aspirating blood clots does not significantly reduce microvascular obstruction or reduce the risk of death in patients with non-ST-elevation myocardial infarction (NSTEMI), when compared to standard percutaneous coronary...

Aspire, Pablo Uceda, DFW Vascular, deep vein thrombosis, thrombectomy
Pablo Uceda, M.D., vascular surgeon with DFW Vascular, Dallas, Texas, was successful in using a new device to clear blood clots out of a patient's legs.
VTEC, NYU Langone, venous therapies, deep vein thrombosis, DVT, PE
NYU Langone Medical Center has announced the creation of a new multidisciplinary Venous Thromboembolic Disease Center (VTEC) to treat those with life...
Covidien, Trellis peripheral infusion system, FDA recall, balloon inflation port
A manufacturing error caused the balloon inflation ports to be mislabeled on Covidien’s Trellis 6 and Trellis 8 Peripheral Infusion systems, prompting a U.S....
Covidien, Solitaire, stent thrombectomy, trial, Netherlands
In a landmark study evaluating the addition of stent thrombectomy clot removal to pharmaceutical treatment for patients suffering an acute ischemic stroke (AIS...
Covidien announced's next-generation Trellis peripheral infusion system is a pharmacomechanical thrombolysis device that enables focused
Ekos Corp.'s EkoSonic endovascular system is for the ultrasound-facilitated, controlled and selective infusion of physician-specified...
The CelanerXT rotational thrombectomy system is a new addition to the Argon Medical Devices Inc.'s Cleaner family of dialysis products....
Medtronic Inc.'s Export Advance aspiration catheter is a U.S. Food and Drug Administration (FDA)-cleared catheter that features a pre-...

Articles

VTEC, NYU Langone, venous therapies, deep vein thrombosis, DVT, PE
NYU Langone Medical Center has announced the creation of a new multidisciplinary Venous Thromboembolic Disease Center (VTEC) to treat those with life...
Stryker, Trevo Retriever, stent thrombectomy, trial, Netherlands
In a landmark study evaluating the addition of stent thrombectomy clot removal to pharmaceutical treatment for patients suffering an acute ischemic stroke (AIS...
Ekos for PE
Acute intermediate-risk pulmonary emboli (PE) in normotensive patients with right ventricle dysfunction present the clinician with a quandary. With a 3 percent...
May 27, 2014 — Ekos Corp. announced the U.S. Food and Drug Administration (FDA) has cleared the EkoSonic endovascular system for the ultrasound-...

Video Center

The biggest technology news coming out of the 2015 American College of Cardiology (ACC) annual...
3 days 10 hours ago
It’s been no secret that the American healthcare system needed to change to survive economically...
6 weeks 3 days ago
The silence is deafening. And since radiology associations, physician groups and vendors have yet...
8 weeks 3 days ago
Centricity, webinar, ZFV, ZFP, viewer, remote viewing system, enterprise
Healthcare organizations are demanding more capabilities for image viewers accessed by clinicians. Zero footprint (ZFP) viewers provide imaging tools from...
The webinar "State of the Art in MRI Pediatric Brain Perfusion Imaging" educates participants about the state of the art clinical and emerging translational...
This webinar discusses why contemporary adult cardiac interventions require significant ionizing radiation with potential health risks to both the patient and...

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