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FDA 510(k)

Community Containers (Flap and Daisy)

Número K: K252637 · 2025-10-14

RequerenteKeter Canada, Inc.
Data da decisão2025-10-14
Código do produtoMMK
Comité consultivoHO
DecisãoSubstantially Equivalent

Resumo do dispositivo

Community Containers (Flap and Daisy) is the device name listed in this FDA 510(k) record. The listed applicant is Keter Canada, Inc.. It received FDA 510(k) clearance on 2025-10-14 under 510(k) number K252637. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Community Containers (Flap and Daisy)?

Community Containers (Flap and Daisy) is a medical device that received FDA 510(k) clearance on 2025-10-14. The listed applicant is Keter Canada, Inc.. The 510(k) number is K252637.

When did Community Containers (Flap and Daisy) receive FDA 510(k) clearance?

Community Containers (Flap and Daisy) received FDA 510(k) clearance on 2025-10-14, under 510(k) number K252637.

Who is the listed applicant for Community Containers (Flap and Daisy)?

The FDA 510(k) record lists Keter Canada, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Community Containers (Flap and Daisy)?

The FDA product code for Community Containers (Flap and Daisy) is MMK.

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