Covidien, LLC( Formerly Beacon Endoscopic Corp.) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covidien, LLC( Formerly Beacon Endoscopic Corp.) - FDA 510(k) Cleared...
2
Total
2
Cleared
0
Denied
Covidien, LLC( Formerly Beacon Endoscopic Corp.) has 2 FDA 510(k) cleared medical devices. Based in Auburndale, US.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Covidien, LLC( Formerly Beacon Endoscopic Corp.) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Covidien, LLC( Formerly Beacon Endoscopic Corp.)
2 devices