FDA 510(k)

Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays

Número K: K222440 · 2022-09-09

RequerenteSteris

Data da decisão2022-09-09

Código do produtoFRG

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays is the device name listed in this FDA 510(k) record. The listed applicant is Steris. It received FDA 510(k) clearance on 2022-09-09 under 510(k) number K222440. 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 Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays?

Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays is a medical device that received FDA 510(k) clearance on 2022-09-09. The listed applicant is Steris. The 510(k) number is K222440.

When did Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays receive FDA 510(k) clearance?

Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays received FDA 510(k) clearance on 2022-09-09, under 510(k) number K222440.

Who is the listed applicant for Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays?

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

What is the FDA product code for Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays?

The FDA product code for Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization Trays is FRG.

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Fonte oficial

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