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First Medical Devices Corp.

United StatesFDA applicant, unverified

Devices
7

What First Medical Devices Corp. makes

First Medical Devices Corp. manufactures manual defibrillators, including the HEARTSTART 2000 series, and ECG-based defibrillator testers such as the FIRST MEDIC Model 610P and its modified variants. These devices are designed for cardiac emergency response, including testing and maintenance of defibrillator functionality.

The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class II and Class III. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does First Medical Devices Corp. have in the registry?

The registry currently lists 7 devices for First Medical Devices Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list First Medical Devices Corp.'s devices?

Among its 7 most recently registered devices, First Medical Devices Corp. has devices listed in FDA 510(k) (7 devices).

What risk classes do First Medical Devices Corp.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for First Medical Devices Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from First Medical Devices Corp. in the registry?

The most recently registered devices listed for First Medical Devices Corp. include HEARTSTART 2000, MANUAL DEFIBRILLATOR, FIRST MEDIC MODEL 610P, HEARTSTART 2000 DEFIBRILLATOR TESTER, ECG and FIRST MEDIC MODE 610.

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