FDA 510(k)

Sterilization Package/Reel

Número K: K241565 · 2025-02-24

RequerenteAnqing Clean Dental Instrument Technology Co., Ltd.

Data da decisão2025-02-24

Código do produtoFRG

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Sterilization Package/Reel is the device name listed in this FDA 510(k) record. The listed applicant is Anqing Clean Dental Instrument Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-02-24 under 510(k) number K241565. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Sterilization Package/Reel?

Sterilization Package/Reel is a medical device that received FDA 510(k) clearance on 2025-02-24. The listed applicant is Anqing Clean Dental Instrument Technology Co., Ltd.. The 510(k) number is K241565.

When did Sterilization Package/Reel receive FDA 510(k) clearance?

Sterilization Package/Reel received FDA 510(k) clearance on 2025-02-24, under 510(k) number K241565.

Who is the listed applicant for Sterilization Package/Reel?

The FDA 510(k) record lists Anqing Clean Dental Instrument Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sterilization Package/Reel?

The FDA product code for Sterilization Package/Reel is FRG.

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Dispositivos Relacionados (Código: FRG)

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Fonte oficial

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