510(k) Report

FDA applicant

Cardiologs Technologies

Paris, FR2 decisions2017–20210 recalls

FDA records 2 decisions for Cardiologs Technologies (Paris, FR) from 2017 to 2021: 2 510(k) clearances. All are in product code DPS (Electrocardiograph). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Cardiologs Technologies’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2017: 12021: 1
2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Cardiologs Technologies by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DPSElectrocardiograph2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 10 times; 1 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K212112Cardiologs Holter PlatformCardiologs Technologies · 20215cite it
  • K170568CardioLogs ECG Analysis PlatformCardiologs Technologies · 20175cite it

What has FDA decided for it lately?

  • K212112Cardiologs Holter PlatformCardiologs Technologies · 2021
  • K170568CardioLogs ECG Analysis PlatformCardiologs Technologies · 2017

All 2 as Cardiologs Technologies →