FDA applicant

Biosensor Corp.

Minneapolis, MN10 decisions1983–19990 recalls

FDA records 10 decisions for Biosensor Corp. (Minneapolis, MN) from 1983 to 1999: 10 510(k) clearances. Most are in product codes DQK (Computer, Diagnostic, Programmable) and DSI (Detector And Alarm, Arrhythmia). 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 Biosensor Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biosensor Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Biosensor Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Biosensor Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?