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 Hewlett-Packard Co., Edan Instruments, Inc. and Ge Medical Systems Information Technologies, Inc..
575
Total
575
Cleared
136d
Avg days
1976
Since
575 devices
Cleared
Nov 26, 1980
MODEL 4700A ELECTROCARDIOGRAPH
Hewlett-Packard Co.
Cardiovascular
26d
Cleared
Jun 11, 1979
MODEL 78501A PATIENT MONITORING SYSTEM
Hewlett-Packard Co.
Cardiovascular
24d
Cleared
Nov 03, 1977
ELAPSED TIME INDICATOR MODEL 21361A
Hewlett-Packard Co.
Cardiovascular
100d
Cleared
May 06, 1977
MONITOR, PORTABLE, PATIENT, G.E.
General Electric Co.
Cardiovascular
11d
Cleared
Sep 09, 1976
ELECTROCARDIOGRAPH (#1505A)
Hewlett-Packard Co.
Cardiovascular
10d
Cleared
Aug 30, 1976
STRESS SYSTEM, SINGLE-CHANNEL (#21125)
Hewlett-Packard Co.
Cardiovascular
12d
Cleared
Aug 30, 1976
STRESS SYSTEM, 3-CHANNEL (#21127A)
Hewlett-Packard Co.
Cardiovascular
12d
Cleared
Jul 19, 1976
MONITOR, PATIENT (MODEL 78331A)
Hewlett-Packard Co.
Cardiovascular
18d