Posted on 8/20/2020
COLUMBIA, MD – July 20, 2020 – Ambu Inc., a rapidly growing medical device maker and pioneer of sterile, single-use endoscopes, announced today that the Ambu® aScope™ Duodeno has received 510(k) clearance from the U.S. Food and Drug Administration (FDA).
At Ambu, we are determined to advance patient safety through innovative design of single-use devices, and we are excited to improve safety for the 2 million patients each year who require an ERCP (Endoscopic Retrograde Cholangio-Pancreatography) procedure,” said Juan Jose Gonzalez, CEO of Ambu A/S, which is based in Copenhagen, Denmark. “It’s no longer necessary to balan...