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M.A. Bioproducts

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Devices
12

Catalogue12

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  • Herpelisa Kit Ref K822883

    Class II
    Active 510(k) 510(k) II

  • Chlamydelisa Test Kit Ref K821967

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

  • Mycoplasmelisa Test Kit Ref K823804

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

  • Cell Culture Reagents Ref K812531

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

  • Cytomegelisa Test Kit Ref K812123

    Not classified
    Active 510(k) 510(k) —

  • Measelisa Test Kit Ref K821762

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

  • Digoxin Eia Kit Ref K801490

    Class II
    Active 510(k) 510(k) II

  • Rubelisa Igm Test Kit Ref K802508

    Class II
    Active 510(k) 510(k) II

  • Varicelisa Test Kit Ref K823805

    Class II
    Active 510(k) 510(k) II

  • Mumpselisa Test Kit Ref K830045

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

  • Toxoelisa Test Kit Ref K813221

    Class II
    Active 510(k) 510(k) II

  • Cytomegelisa Stat Ref K830615

    Class II
    Active 510(k) 510(k) II

Rows 1-12 of 12

Frequently asked questions

How many devices does M.A. Bioproducts have in the registry?

The registry currently lists 12 devices for M.A. Bioproducts. Devices recorded under merged duplicate company entries are counted once.

Which registries list M.A. Bioproducts's devices?

Among its 12 most recently registered devices, M.A. Bioproducts has devices listed in FDA 510(k) (12 devices).

What risk classes do M.A. Bioproducts's devices fall under?

Among its 12 most recently registered devices, the classes recorded for M.A. Bioproducts's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from M.A. Bioproducts in the registry?

The most recently registered devices listed for M.A. Bioproducts include HERPELISA KIT, CHLAMYDELISA TEST KIT, MYCOPLASMELISA TEST KIT and CELL CULTURE REAGENTS.

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