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Cambridge Multi-Draw, Inc.

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Devices
1

What Cambridge Multi-Draw, Inc. makes

Cambridge Multi-Draw, Inc. manufactures the MultiDraw System, a medical device designed for repeated sampling or fluid extraction in clinical or procedural settings.

The MultiDraw System is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Multidraw System Ref K922858

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

Frequently asked questions

How many devices does Cambridge Multi-Draw, Inc. have in the registry?

The registry currently lists 1 device for Cambridge Multi-Draw, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cambridge Multi-Draw, Inc.'s devices?

Among its 1 most recently registered device, Cambridge Multi-Draw, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Cambridge Multi-Draw, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Cambridge Multi-Draw, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cambridge Multi-Draw, Inc. in the registry?

The most recently registered devices listed for Cambridge Multi-Draw, Inc. include MULTIDRAW SYSTEM.

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