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Dilab, Inc.

United StatesFDA applicant, unverified

Devices
11

Catalogue11

Newest first, rows 1-11 of 11

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  • Rapid As Latex Ref K862530

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

  • Total Proteins Ref K850936

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

  • Calcium Ref K850929

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

  • Phosphorus Ref K850934

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

  • Albumin Ref K850931

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

  • Chloride Ref K850935

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

  • Creatinine Ref K850932

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

  • Uric Acid Ref K850933

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

  • Cholesterol Ref K850938

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

  • Urea Ref K850937

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

  • Glucose Ref K850930

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

Rows 1-11 of 11

Frequently asked questions

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

The registry currently lists 11 devices for Dilab, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dilab, Inc.'s devices?

Among its 11 most recently registered devices, Dilab, Inc. has devices listed in FDA 510(k) (11 devices).

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

Among its 11 most recently registered devices, the classes recorded for Dilab, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Dilab, Inc. include RAPID AS LATEX, TOTAL PROTEINS, CALCIUM and PHOSPHORUS.

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