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21,775 catalysts · 4,728 grant · 3,740 device 510k · 3,706 8k filing · 3,020 approval · 2,000 device pma · 2,000 device recall
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21,775 catalysts · 4,728 grant · 3,740 device 510k · 3,706 8k filing · 3,020 approval · 2,000 device pma · 2,000 device recall
Adverse Event Without Identified Device or Use Problem
Signal Artifact/Noise; Electromagnetic Interference
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Signal Artifact/Noise; Fracture
Patient Device Interaction Problem
Patient Device Interaction Problem
Material Rupture
Difficult to Remove
Insufficient Flow or Under Infusion
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Device Appears to Trigger Rejection
Insufficient Flow or Under Infusion
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Wireless Communication Problem
Insufficient Information
Use of Device Problem
Appropriate Term/Code Not Available
Insufficient Flow or Under Infusion
Use of Device Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Migration
Over-Sensing; High Capture Threshold
Adverse Event Without Identified Device or Use Problem
Fracture
Complete Blockage
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Excess Flow or Over-Infusion