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Physical Diagnostics, Inc.

Country not established

Devices
1

What Physical Diagnostics, Inc. makes

Physical Diagnostics, Inc. manufactures the TPG 1000, a device designed for physical diagnostic testing, likely related to respiratory or pulmonary function assessment.

The TPG 1000 is classified as a Class I medical device and is listed under FDA’s 510(k) pathway. The company 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

  • Tpg 1000 Ref K831002

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

Frequently asked questions

How many devices does Physical Diagnostics, Inc. have in the registry?

The registry currently lists 1 device for Physical Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Physical Diagnostics, Inc.'s devices?

Among its 1 most recently registered device, Physical Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Physical Diagnostics, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Physical Diagnostics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Physical Diagnostics, Inc. in the registry?

The most recently registered devices listed for Physical Diagnostics, Inc. include TPG 1000.

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