Electrocardiograph
FDA product code DPS · Class 2 · 307 devices · 343 reports · 2 deaths reported · 263 devices named in recalls
- M SERIES BIPHASIC 40010511100163010Zoll Medical Corporation · ELECTROCARDIOGRAPH1 report
- M SERIES BIPHASIC 40021511110123010Zoll Medical Corporation · ELECTROCARDIOGRAPH1 report
- M SERIES BIPHASIC 40021711110163010Zoll Medical Corporation · ELECTROCARDIOGRAPH1 report
- M SERIES BIPHASIC 60010011100010011Zoll Medical Corporation · ELECTROCARDIOGRAPH1 report
- M SERIES BIPHASIC 60010011100063010Zoll Medical Corporation · ELECTROCARDIOGRAPH1 report
- CARDIOVIT® FT-1 3.900863Schiller AG · Electrocardiograph1 report
- MR Patient Care Single Patch ECG Electrodes (25) QUADTRODE MRI ECG PAD,25/BOXPhilips Ds North America LLC · ELECTROCARDIOGRAPH1 report