Teleflex: FDA Clears Arrow EZ-IO Needle As MR Conditional
(RTTNews) - Teleflex Incorporated (TFX) announced FDA 510(k) clearance of Arrow EZ-IO Needle for MR conditional safety status labeling. The company said the new labeling allows the clinician to continuously care for patients who require MRI scans without interruption to the established site for vascular access.
The EZ-IO Needle is a critical component of the Arrow EZ-IO Intraosseous Vascular Access System. The EZ-IO System can be used when intravenous access is difficult in emergent, urgent, or medically necessary cases.
Michelle Fox, Corporate Vice President and Chief Medical Officer, said: "Patients who require emergent or urgent MRI now have an additional vascular access option."
For More Such Health News, visit rttnews.com.
Founded in the late 1990s by Andrew Mariathasan in New York, with the goal of covering Wall Street for a new generation of investors, RTTNews has expanded steadily over the years to become a trusted provider of content for a wide array of subjects across several platforms. RTT's Financial Newswire is relied upon by some of the world's largest financial institutions, including banks, brokerages, trading platforms and financial exchanges.