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Maryrose Cusimano, Ph.D./Phil Reaston

Country not established

Devices
1

What Maryrose Cusimano, Ph.D./Phil Reaston makes

The company produces a Physical Monitoring Registration Unit, a device designed for tracking and recording physiological data in clinical or research settings.

This device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Maryrose Cusimano, Ph.D./Phil Reaston have in the registry?

The registry currently lists 1 device for Maryrose Cusimano, Ph.D./Phil Reaston. Devices recorded under merged duplicate company entries are counted once.

Which registries list Maryrose Cusimano, Ph.D./Phil Reaston's devices?

Among its 1 most recently registered device, Maryrose Cusimano, Ph.D./Phil Reaston has devices listed in FDA 510(k) (1 device).

What risk classes do Maryrose Cusimano, Ph.D./Phil Reaston's devices fall under?

Among its 1 most recently registered device, the classes recorded for Maryrose Cusimano, Ph.D./Phil Reaston's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Maryrose Cusimano, Ph.D./Phil Reaston in the registry?

The most recently registered devices listed for Maryrose Cusimano, Ph.D./Phil Reaston include PHYSICAL MONITORING REGISTRATION UNIT.

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