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Chase Medical, LP

United StatesFDA applicant, unverified

Devices
2

What Chase Medical, LP makes

Chase Medical, LP manufactures the CHASE CARDIAC ANALYSIS SYSTEM and the CHASE MR SYSTEM, both of which are medical devices.

These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the US.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Chase Cardiac Analysis System Ref K062031

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Chase Mr System Ref K072473

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

Frequently asked questions

How many devices does Chase Medical, LP have in the registry?

The registry currently lists 2 devices for Chase Medical, LP. Devices recorded under merged duplicate company entries are counted once.

Which registries list Chase Medical, LP's devices?

Among its 2 most recently registered devices, Chase Medical, LP has devices listed in FDA 510(k) (2 devices).

What risk classes do Chase Medical, LP's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Chase Medical, LP's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Chase Medical, LP in the registry?

The most recently registered devices listed for Chase Medical, LP include CHASE CARDIAC ANALYSIS SYSTEM and CHASE MR SYSTEM.

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