FDA applicant

Centrimed Corp.

Hopkins, MN4 decisions1984–19850 recalls

FDA records 4 decisions for Centrimed Corp. (Hopkins, MN) from 1984 to 1985: 4 510(k) clearances. Most are in product codes KFM (Pump, Blood, Cardiopulmonary Bypass…) and DTQ (Console, Heart-Lung Machine, Cardiopulmonary…). 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 Centrimed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Centrimed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Centrimed Corp.

Which product codes does it file in?

What has FDA decided for it lately?