FDA applicant

S & W Medico Teknik

Denmark, DK46 decisions1984–19950 recalls

FDA records 46 decisions for S & W Medico Teknik (Denmark, DK) from 1984 to 1995: 46 510(k) clearances. Most are in product codes DRT (Monitor, Cardiac (Incl. Cardiotachometer &…) and DRX (Electrode, Electrocardiograph). 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 S & W Medico Teknik’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for S & W Medico Teknik since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — S & W Medico Teknik by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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S & W Medico Teknik

Which product codes does it file in?

What has FDA decided for it lately?