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Kt Medical, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
13

Catalogue13

Newest first, rows 1-13 of 13

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  • Combison 100-Model 100 & 110 Ref K800091

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

  • Model E03 Echo-Opthalmoscope Ref K800652

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

  • 4200 Me Echoencephalograph Ref K800101

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

  • Combison 200 & Combison 202 Ref K800094

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

  • Transducer Ref K800093

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

  • Sinvision Linear Array Real Time Ref K800653

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

  • Minivason 9 Ref K800097

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

  • Intracula Ii Ref K800099

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

  • Ambivason Dr-200 Ref K800096

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

  • Minifeton 200 Ref K800098

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

  • Combison Computer Ref K800092

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

  • Mgd-3 Ref K800095

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

  • 7200 Ma Echo-Ophthalmoscope Ref K800100

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

Rows 1-13 of 13

Frequently asked questions

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

The registry currently lists 13 devices for Kt Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kt Medical, Inc.'s devices?

Among its 13 most recently registered devices, Kt Medical, Inc. has devices listed in FDA 510(k) (13 devices).

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

Among its 13 most recently registered devices, the classes recorded for Kt Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Kt Medical, Inc. include COMBISON 100-MODEL 100 & 110, MODEL E03 ECHO-OPTHALMOSCOPE, 4200 ME ECHOENCEPHALOGRAPH and COMBISON 200 & COMBISON 202.

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