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Intratherapeutics, Inc.

United StatesFDA applicant, unverified

Devices
15

Catalogue15

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Frequently asked questions

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

The registry currently lists 15 devices for Intratherapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Intratherapeutics, Inc.'s devices?

Among its 15 most recently registered devices, Intratherapeutics, Inc. has devices listed in FDA 510(k) (15 devices).

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

Among its 15 most recently registered devices, the classes recorded for Intratherapeutics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Intratherapeutics, Inc. include INTRACOIL PERIPHERAL STENT, INTRASTENT DOUBLESTRUT PARAMOUNT BILIARY ENDOPROSTHESIS, ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65 and INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY.

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