Medical Device Manufacturer · US , Mansfield , MA

Covidien Lp, Formerly Registered AS Kendall - FDA 510(k) Cleared Devi...

3 submissions · 2 cleared · Since 2009
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.

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All3 Gastroenterology & Urology 2 General Hospital 1