Boston Endoscopic Engineering is one of 15082 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Boston Endoscopic Engineering - FDA 510(k) Cleared Devices
Recent clearances: BNX FINE NEEDLE ASPIRATION SYSTEM
1
Total
1
Cleared
0
Denied
Boston Endoscopic Engineering has 1 FDA 510(k) cleared medical devices. Based in Foster, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Boston Endoscopic Engineering Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Boston Endoscopic Engineering
1 devices