Covidien, LLC( Formerly Beacon Endoscopic Corp.) is one of 5098 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.
Covidien, LLC( Formerly Beacon Endoscopic Corp.) — FDA 510(k) Products and Clearance History
2 devices
Cleared
May 01, 2015
BNX Fine Needle Aspiration System and SharkCore LG Fine Needle Biopsy System
General & Plastic Surgery
29d
Cleared
Oct 06, 2014
SHARKCORE FINE NEEDLE BIOPSY SYSTEM
Gastroenterology & Urology
84d