Jan. 23, 2007 — Vascular Solutions announced it has received 510(k) clearance from the FDA to begin marketing its new ...
Cath Lab
The catheterization lab channel includes content related to interventional technologies for coronary and peripheral artery disease (PAD). Other cath lab transcatheter device technologies covered on this page included percutaneous treatment for stroke, venous interventions, heart valves, hypertension, heart failure and percutenous coronary interventions (PCI).
Jan. 23, 2007 — The FDA has granted 510(k) clearance for FlowCardia’s CROSSER 14 CTO Recannalization System, an ...
Jan. 19, 2007 — Biosense Webster made two agreements public this week with healthcare competitor modality giants ...
Adjustable parameters on the ACIST® CVI® Contrast Delivery System include, flow rate, volume, pressure limit, rise time ...
Jan. 19, 2007 — The second generation Coating Durability Tester (CDT2) by Dynatek will be exhibited at the Medical ...
Jan. 15, 2007 — Boston Scientific Corp. has announced the international launch and first implantation of the PROMUS ...
Jan. 11, 2007 — AngioScore’s flagship product, the AngioSculpt Scoring Balloon Catheter, has received FDA Premarket ...
As medical advancements continue to push the boundaries of what is possible in the field of structural heart ...
Jan. 11, 2007 — The Society for Cardiovascular Angiography and Interventions (SCAI) today released a clinical alert ...
January 9, 2007 - Konica Minolta Medical Imaging announced that it has been awarded contract positions with ...
Jan. 5, 2007 — A French court has ruled that Abbott Laboratories’ Xience V drug-eluting coronary stents infringe patents ...
While the current positive revolution in percutaneous coronary intervention (PCI) practice has been made possible by the ...
Implant Sciences Corp. a wholly-owned German subsidiary of CorNova, Inc., has received CE Mark marketing approval for ...
Swiss researchers may have discovered the reason drug-eluting stents cause thrombosis, and their study results are ...
The latest in thrombus removal devices from Possis has received FDA clearance — the new AngioJet Ultra ...
During cardiology fellowship, my institution had a hand manifold system. I found it difficult to use at times, and it ...
The FDA has granted 510(k) marketing clearance for Atrium Medical Corp.’s ClearWay RX, a therapeutic perfusion catheter ...
UnitedHealthcare has announced its support for the “Door to Balloon (D2B): An Alliance for Quality” campaign ...
In a new, five-year agreement signed last week, Datascope’s InterVascular Division will become the distributor of Sorin ...