Data / Medical devices / Electrocardiograph

Electrocardiograph (DPS): 129 FDA-registered makers in 22 countries

129 establishments in 22 countries are registered with the FDA to make Electrocardiograph (product code DPS, Class 2, 21 CFR 870.2340). 65 of them have a 510(k) clearance or PMA approval on file and 9 have a recall event. The FDA has issued 579 510(k) clearances under this code, the latest on October 23, 2026, and lists 34 recall events (1 Class I). FDA data exported November 2, 2026.

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Product code

DPS

Device class

2

Regulation

870.2340

Medical specialty

Cardiovascular

Makers by country

Makers of Electrocardiograph

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated October 23, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.