Covidien, LLC - FDA 510(k) Cleared Devices
Recent clearances: Tri-Staple™ 2.0 Black Circular Reload 21mm Extra Thick (SIGCIR21XT), Instrument Exit Point on Touch Surgery™ Aide, Capnostream™35 Portable Respiratory Monitor (PM35MN)
90
Total
87
Cleared
1
Denied
FDA 510(k) Regulatory Record - Covidien, LLC Neurology ✕
1 devices