BRIDGEWATER, N.J.--(BUSINESS WIRE)-- Cordis Corporation is pleased to announce the launch of SLEEK® OTW Catheter, a new .014” Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter designed to ...
r4 Vascular has announced it has received FDA clearance for its Vector percutaneous transluminal angioplasty balloon catheters, according to a news release. The catheters are available in 28 sizes.
TAMPA, Fla.--(BUSINESS WIRE)--Concept Medical Inc. (CMI) has been granted "Breakthrough Device Designation" from the U.S. Food and Drug Administration (FDA) for MagicTouch PTA (Percutaneous ...
WAYNE, Pa.--(BUSINESS WIRE)--Intact Vascular, Inc., a developer of medical devices for minimally invasive peripheral vascular procedures, today announced that current investors New Enterprise ...
Outside of his work doing minimally-invasive vascular surgeries, Dr. Charles Sternbergh spends time with his wife, Tasha, and ...
The treatment of patients with peripheral arterial disease has evolved tremendously since the early 1960s, when Charles Dotter first successfully revascularized a superficial femoral artery occlusion ...
PinnacleHealth CardioVascular Institute enrolled the first patient in Pennsylvania into the TOBA II clinical on October 19, 2015. This trial is to assess the safety and efficacy of a vascular implant ...
MyChesCo on MSN
Cagent Vascular Unveils Serranator SL-PRO to Enhance Treatment of Peripheral Artery Disease
WAYNE, PA — Cagent Vascular, Inc. has announced the launch of its latest innovation, the Serranator SL-PRO™ PTA Serration ...
Minnesota's r4 Vascular has secured FDA clearance for its Vector percutaneous transluminal angioplasty balloon catheter, a quick-inflate device rated for up to 30 atmospheres of pressure. The device ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results
Feedback