FDA applicant

Ergometrix, Inc.

Minneapolis, MN1 decision1993–19930 recalls

FDA records 1 decision for Ergometrix, Inc. (Minneapolis, MN) in 1993: 1 510(k) clearance. All are in product code KRI (Accessory Equipment, Cardiopulmonary Bypass). 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 Ergometrix, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ergometrix, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ergometrix, Inc.

Which product codes does it file in?

What has FDA decided for it lately?