DPS · Class II · 21 CFR 870.2340

FDA Product Code DPS: Electrocardiograph

FDA product code DPS covers electrocardiographs used for recording the electrical activity of the heart.

These devices capture and display the cardiac electrical cycle as a series of waveforms — P, QRS, and T waves — that provide diagnostic information about heart rate, rhythm, and conduction. ECG recordings are essential in the diagnosis of arrhythmias, myocardial infarction, and other cardiac conditions.

DPS devices are Class II medical devices, regulated under 21 CFR 870.2340 and reviewed by the FDA Cardiovascular panel.

Leading manufacturers include Nihon Kohden America, Inc., Mortara Instrument, Inc. and Edan Instruments, Inc..

576
Total
576
Cleared
136d
Avg days
1976
Since
576 devices
313–336 of 576
No devices found for this product code.