Medical Device Manufacturer · US , Mounds View , MN

Medtronic, Inc. - FDA 510(k) Cleared Devices

215 submissions · 214 cleared · Since 1981

Recent clearances: DLP™ Coronary Ostial Cannulae, Protégé™ EverFlex™ Self-expanding Peripheral Stent System, LINQ II Insertable Cardiac Monitor (ICM) (LNQ22)

View 215 510(k) Devices ↓ Official Website

215

Total

214

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medtronic, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared May 20, 2016

Temperature Probe, Affinity Temperature Probe

General Hospital · 126d