Teleflex Announced U.S. Food And Drug Administration (FDA) 510(k) Clearance Of The Ringer Perfusion Balloon Catheter, The Only Commercially Available Percutaneous Transluminal Coronary Angioplasty Perfusion Balloon
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Teleflex has received FDA 510(k) clearance for its Ringer Perfusion Balloon Catheter, the only commercially available percutaneous transluminal coronary angioplasty perfusion balloon.
July 31, 2024 | 10:35 am
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Teleflex has received FDA 510(k) clearance for its Ringer Perfusion Balloon Catheter, making it the only commercially available percutaneous transluminal coronary angioplasty perfusion balloon.
The FDA 510(k) clearance is a significant regulatory milestone that allows Teleflex to market its unique Ringer Perfusion Balloon Catheter. This could lead to increased sales and market share in the medical devices sector.
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