Please provide your email address to receive an email when new articles are posted on . The FDA has designated a recall of a peripheral catheter system as class I, the most serious kind. Teleflex and ...

Feb. 23—dbeard @dominionpost.com MORGANTOWN — In the ever-evolving quest to improve treatment for stroke victims, WVU Rockefeller Neuroscience Institute recently performed the first in-human procedure ...

New Peripheral Line Draw Solution Delivers First and Only Compatibility with Integrated Catheters, Bringing Elevated Standard of Care to More U.S. Hospitals With 510(k) clearance from the U.S. Food ...

Researchers have developed a device that offers a quicker and less invasive way to seal tears and holes in blood vessels, using an electrically-activated glue patch applied via a minimally invasive ...

WAYNE, Pa. & TULLINGE, Sweden--(BUSINESS WIRE)--XyloCor Therapeutics, Inc. (“XyloCor”), a clinical‑stage biopharmaceutical company developing novel gene therapies for cardiovascular disease, and ...

InterVene’s Recana, a mechanical thrombectomy catheter designed to address venous in-stent restenosis (ISR) and clear vessel obstructions, has received 510(k) clearance from the US Food and Drug ...

BD is building on its goal of providing patients with a “one-stick hospital stay” with a new FDA clearance for painless blood collection hardware that works through already placed IV lines. The ...

Kalamazoo, MI – Ablative Solutions, Inc., a privately-held clinical stage company, announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its ...

A "fuzzy logic" alarm system may help nurses in the neonatal intensive care unit (NICU) predict impending catheter infusion failure – and prevent complications in critically ill newborns, reports a ...

A team of researchers led by Nanyang Technological University, Singapore (NTU Singapore) has developed a device that offers a quicker and less invasive way to seal tears and holes in blood vessels, ...