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Cytochem, Inc.

Country not established

Devices
1

What Cytochem, Inc. makes

Cytochem, Inc. manufactures the CYTOBUCKET Model 1024, a device designed for handling and processing cytological specimens in laboratory settings. This product is intended to facilitate the preparation of samples for microscopic examination, ensuring proper containment and transport of cytology materials.

The CYTOBUCKET Model 1024 is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Cytobucket Model 1024 Ref K810848

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

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

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

Which registries list Cytochem, Inc.'s devices?

Among its 1 most recently registered device, Cytochem, Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Cytochem, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Cytochem, Inc. include CYTOBUCKET MODEL 1024.

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