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Stentor Inc., A Philips Medical Systems Co.

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Devices
1

What Stentor Inc., A Philips Medical Systems Co. makes

Stentor Inc. develops and maintains the ISITE PACS V 4.X, a picture archiving and communication system (PACS) designed for managing, storing, and distributing medical imaging data within healthcare settings.

The ISITE PACS V 4.X is classified as a Class II medical device in the US and is listed under the 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

  • Isite Pacs, V 4. X Ref K063267

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

Frequently asked questions

How many devices does Stentor Inc., A Philips Medical Systems Co. have in the registry?

The registry currently lists 1 device for Stentor Inc., A Philips Medical Systems Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Stentor Inc., A Philips Medical Systems Co.'s devices?

Among its 1 most recently registered device, Stentor Inc., A Philips Medical Systems Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Stentor Inc., A Philips Medical Systems Co.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Stentor Inc., A Philips Medical Systems Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Stentor Inc., A Philips Medical Systems Co. in the registry?

The most recently registered devices listed for Stentor Inc., A Philips Medical Systems Co. include ISITE PACS, V 4. X.

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