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Syn-Kit, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
34

Catalogue34

Newest first, rows 1-34 of 34

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  • Blf Eiken Kit Deter. Of B-Lipopr. Frac. Ref K802451

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

  • Got Isoenzyme Assay Eiken Kit Ref K802447

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

  • Aso Slide Eiken Ref K853276

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

  • Ra 80 Eiken Kit Determ. Of Rheumatic F. Ref K802448

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

  • Fibrogen(Fibrin Split Product) Antigen Ref K812298

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

  • Uropaper Eiken Uhag Ref K811816

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

  • Uropaper Eiken 5 Ref K843756

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

  • Uropaper Eiken Hag Ref K843759

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

  • Uricase (U.V.) Uric Acid Ref K821167

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

  • Slide Culture U 'eiken' Ref K861631

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

  • Reagent Tests Strip Combinations Ref K833521

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

  • Uropaper Eiken Uag Ref K811818

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

  • Ra 80 Eiken Ref K854820

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

  • Uropaper Eiken 8 Ref K843532

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

  • Systek #1 Eiken Ref K813164

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

  • Uropaper Eikeg Ref K811815

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

  • Uropaper Eiken 7 Ref K843754

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

  • Gestate Slide Eiken Kit Agg. Method Hum Ref K802450

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

  • Trep Card Eiken Ref K820567

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

  • Toxotest-Mt Eiken Kit Ref K802452

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

  • Uropaper Eiken Gk Ref K843758

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

  • Uropaper Eiken AG Ref K811817

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

  • Uropaper Eiken 6B Ref K843755

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

  • Uropaper Eiken AG Ref K843757

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

  • Triglyzyme V Eiken Ref K821106

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

  • Uropaper Eiken Gp Ref K843753

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

  • Seroiden Strepto Kit 'eiken' Ref K861098

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

  • Urine Screening Kit Ref K830824

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

  • Hdl-C Eiken Ref K813192

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

  • Geste Follow Kit Determ. Of Hpl Ref K802454

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

  • Cholestezyme-V Eiken Ref K821105

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

  • Uropaper Eiken G Ref K843760

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

  • Crp Slide Ref K810862

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

  • Cpr Slide Eiken Ref K854819

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

Rows 1-34 of 34

Frequently asked questions

How many devices does Syn-Kit, Inc. have in the registry?

The registry currently lists 34 devices for Syn-Kit, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Syn-Kit, Inc.'s devices?

Among its 34 most recently registered devices, Syn-Kit, Inc. has devices listed in FDA 510(k) (34 devices).

What risk classes do Syn-Kit, Inc.'s devices fall under?

Among its 34 most recently registered devices, the classes recorded for Syn-Kit, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Syn-Kit, Inc. in the registry?

The most recently registered devices listed for Syn-Kit, Inc. include BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC., GOT ISOENZYME ASSAY EIKEN KIT, ASO SLIDE EIKEN and RA 80 EIKEN KIT DETERM. OF RHEUMATIC F..

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