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Potomac Medical System

Country not established

Devices
2

What Potomac Medical System makes

Potomac Medical System manufactures a computerized electro-oculograph, a diagnostic device used to measure eye movements by detecting electrical potentials generated by the retina. They also produce the Metachrome, a device designed for ophthalmic testing, likely involving color vision or retinal analysis.

The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their portfolio is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Computerized Electro-Oculograph Ref K790637

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Metachrome Ref K851174

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

Frequently asked questions

How many devices does Potomac Medical System have in the registry?

The registry currently lists 2 devices for Potomac Medical System. Devices recorded under merged duplicate company entries are counted once.

Which registries list Potomac Medical System's devices?

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

What risk classes do Potomac Medical System's devices fall under?

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

What are the newest devices from Potomac Medical System in the registry?

The most recently registered devices listed for Potomac Medical System include COMPUTERIZED ELECTRO-OCULOGRAPH and METACHROME.

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