A prevention bundle reduced inflammation, infections and hospitalizations among nursing home residents with peripherally ...
The US Food and Drug Administration (FDA) has granted 510(k) clearance to the Neonav electrocardiogram (ECG) tip location system, a central venous access device (CVAD) placement platform developed by ...
Pediatr Crit Care Med. 2013;14(3):273-283 ... The skin is marked to indicate the underlying target vein course, and then venous cannulation is attempted without real-time ultrasound imaging.
Central Venous Catheters All catheters consists of high flexible thin-walled polyurethane which ensures very high flow rates. It is anti-thrombogen and biocompatible.
Imperative Care has received a green light from the FDA for its large-bore catheter to help remove stroke-causing blood clots from within the brain. The new 510(k) clearance expands the portfolio ...
CAMPBELL, Calif.--(BUSINESS WIRE)--Imperative Care, Inc. today announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance of the company’s Zoom System, making it the ...
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