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Cardiac Resucitator Corp.

United StatesFDA applicant, unverified

Devices
17

What Cardiac Resucitator Corp. makes

Cardiac Resuscitator Corp. manufactures external defibrillators, including automated and manual models designed for emergency cardiac resuscitation, such as the Modified Heart*Aid 97 Auto and Heart*Aid 1000. Their portfolio also includes pacemaker devices, including models like the PACE*AID 10A and PACE*AID Model 53, which regulate heart rhythms and feature output displays. Additional products include standalone pacemakers and defibrillator units like the Heart-Aid Model 80 and PACE*AID.

The company’s devices are classified under FDA categories Class II and Class III, reflecting varying levels of regulatory oversight for pacemakers and defibrillators. These products are listed via the FDA’s 510(k) pathway, demonstrating compliance with pre-market notification requirements. The manufacturer operates from the United States, adhering to domestic regulatory standards for medical electrical devices.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue17

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  • Modified Heart*aid 97 Auto. External Defibrillator Ref K871569

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pace* Aid Model 50 Ref K820507

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pace*aid 10 A -Pad 10A- Pacemaker Output Display & Ref K850596

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart Aid Model 97 Ref K850170

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart*aid 1000 Ref K870622

    Active Regimes: 510(k) Registry: 510(k) Class:III

  • Modified Heart*aid 97 Auto. External Defibrillator Ref K882513

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pace Aid Ref K811028

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Modified Pace*aid Model 53 Ref K871971

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart Aid #90 Ref K821152

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pace Aid Model 53 Ref K844811

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart-Aid Model 80 Ref K843358

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pace *aid Ref K813553

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Stat-Pad (Tm) Ref K871538

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart - Aid Als, 95 Ref K841556

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart *aid, #80 Ref K820609

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Heart*aid, Als, Model 95 Ref K821673

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pace *aid Model 52 Ref K843547

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-17 of 17

Frequently asked questions

How many devices does Cardiac Resucitator Corp. have in the registry?

The registry currently lists 17 devices for Cardiac Resucitator Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cardiac Resucitator Corp.'s devices?

Among its 17 most recently registered devices, Cardiac Resucitator Corp. has devices listed in FDA 510(k) (17 devices).

What risk classes do Cardiac Resucitator Corp.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for Cardiac Resucitator Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Cardiac Resucitator Corp. in the registry?

The most recently registered devices listed for Cardiac Resucitator Corp. include MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR, PACE* AID MODEL 50, PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY & and HEART AID MODEL 97.

Generated automatically from registry data and not verified by a human reviewer.