FDA applicant

Cardiac Resucitator Corp.

Mchenry, IL17 decisions1981–19880 recalls

FDA records 17 decisions for Cardiac Resucitator Corp. (Mchenry, IL) from 1981 to 1988: 17 510(k) clearances. Most are in product codes DRO (Pacemaker, Cardiac, External Transcutaneous…) and MKJ (Automated External Defibrillators (Non-Wearable)). 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 Cardiac Resucitator Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cardiac Resucitator Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cardiac Resucitator Corp.

Which product codes does it file in?

What has FDA decided for it lately?