Product code DRF— Cardiovascular

IntellaMap Orion High Resolution Mapping Catheter

Classification name
Catheter, Electrode Recording, Or Probe, Electrode Recording
Device class
Class 2
Regulation
21 CFR 870.1220
Advisory panel
Cardiovascular
Total cleared
186
First cleared
Most recent

Clearances under product code DRF — page 2

101–186 of 186

Data sourced from openFDA. This site is unofficial and independent of the FDA.