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Lockett Medical Corp.

United StatesFDA applicant, unverified

Devices
3

Catalogue3

Newest first, rows 1-3 of 3

  • Sterile Water O.9% Sterile Saline Ref K954887

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Lockett Medical Corp. Gauze Ref K950404

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Reusable Glass Syringes Ref K011176

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Lockett Medical Corp. have in the registry?

The registry currently lists 3 devices for Lockett Medical Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lockett Medical Corp.'s devices?

Among its 3 most recently registered devices, Lockett Medical Corp. has devices listed in FDA 510(k) (3 devices).

What risk classes do Lockett Medical Corp.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Lockett Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Lockett Medical Corp. in the registry?

The most recently registered devices listed for Lockett Medical Corp. include STERILE WATER O.9% STERILE SALINE, LOCKETT MEDICAL CORP. GAUZE and REUSABLE GLASS SYRINGES.

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