FDA 510(k)

enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System

Número K: K243433 · 2024-12-02

Data da decisão2024-12-02

Código do produtoFEB

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2024-12-02 under 510(k) number K243433. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System?

enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System is a medical device that received FDA 510(k) clearance on 2024-12-02. The listed applicant is STERIS Corporation. The 510(k) number is K243433.

When did enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System receive FDA 510(k) clearance?

enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System received FDA 510(k) clearance on 2024-12-02, under 510(k) number K243433.

Who is the listed applicant for enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System?

The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System?

The FDA product code for enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System is FEB.

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Outros registros que listam STERIS Corporation como candidato(a)

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Fonte oficial

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