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Ezmt Valve Co., Inc.

United StatesFDA 510(k) applicant, unverified

Devices
3

Catalogue3

Newest first, rows 1-3 of 3

  • Latex Examination Glove Ref K930557

    Class I
    Active 510(k) 510(k) I
  • Leg Urinal Ref K913155

    Class II
    Active 510(k) 510(k) II
  • Night Urinary Drainage Bedside Bag Ref K930556

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

Frequently asked questions

How many devices does Ezmt Valve Co., Inc. have in the registry?

The registry currently lists 3 devices for Ezmt Valve Co., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ezmt Valve Co., Inc.'s devices?

Among its 3 most recently registered devices, Ezmt Valve Co., Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Ezmt Valve Co., Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Ezmt Valve Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ezmt Valve Co., Inc. in the registry?

The most recently registered devices listed for Ezmt Valve Co., Inc. include LATEX EXAMINATION GLOVE, LEG URINAL and NIGHT URINARY DRAINAGE BEDSIDE BAG.

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