FDA applicant

Cardio Search, Inc.

Walker, MI5 decisions1983–19930 recalls

FDA records 5 decisions for Cardio Search, Inc. (Walker, MI) from 1983 to 1993: 5 510(k) clearances. Most are in product codes DQY (Catheter, Percutaneous) and FOZ (Catheter, Intravascular, Therapeutic…). No recall is linked to its devices.

FDA’s records also spell it “Cardio-Search , Ltd.”.

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 Cardio Search, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cardio Search, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cardio Search, Inc.

Which product codes does it file in?

What has FDA decided for it lately?