Covidien Lp, Formerly Registered AS Kendall - FDA 510(k) Cleared Devi...
3
Total
2
Cleared
0
Denied
Covidien Lp, Formerly Registered AS Kendall has 2 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 2 cleared submissions from 2009 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Covidien Lp, Formerly Registered AS Kendall Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Covidien Lp, Formerly Registered AS...
3 devices