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Accu Science Corp.

United StatesFDA applicant, unverified

Devices
2

What Accu Science Corp. makes

Accu Science Corp. makes the Acculator 287EP and Acculator 487E devices.

These devices are Class II medical devices listed in the FDA 510(k) registry and the company is based in the United States.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Acculator 287EP Ref K871396

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Acculator 487E Ref K862352

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

Frequently asked questions

How many devices does Accu Science Corp. have in the registry?

The registry currently lists 2 devices for Accu Science Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Accu Science Corp.'s devices?

Among its 2 most recently registered devices, Accu Science Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Accu Science Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Accu Science Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Accu Science Corp. in the registry?

The most recently registered devices listed for Accu Science Corp. include ACCULATOR 287EP and ACCULATOR 487E.

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