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The Home Emergency Room

Country not established

Devices
1

What The Home Emergency Room makes

The Home Emergency Room manufactures first aid kits designed for home use, containing essential medical supplies for minor injuries and emergencies.

These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records in the US.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • First Aid Kit Ref K921976

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

Frequently asked questions

How many devices does The Home Emergency Room have in the registry?

The registry currently lists 1 device for The Home Emergency Room. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Home Emergency Room's devices?

Among its 1 most recently registered device, The Home Emergency Room has devices listed in FDA 510(k) (1 device).

What risk classes do The Home Emergency Room's devices fall under?

Among its 1 most recently registered device, the classes recorded for The Home Emergency Room's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from The Home Emergency Room in the registry?

The most recently registered devices listed for The Home Emergency Room include FIRST AID KIT.

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