FDA 510(k)

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses

Número K: K173136 · 2017-11-16

Data da decisão2017-11-16

Código do produtoMRC

Comité consultivoOP

DecisãoSubstantially Equivalent

Resumo do dispositivo

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is the device name listed in this FDA 510(k) record. The listed applicant is Menicon Co, Ltd.. It received FDA 510(k) clearance on 2017-11-16 under 510(k) number K173136. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is a medical device that received FDA 510(k) clearance on 2017-11-16. The listed applicant is Menicon Co, Ltd.. The 510(k) number is K173136.

When did Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses receive FDA 510(k) clearance?

Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses received FDA 510(k) clearance on 2017-11-16, under 510(k) number K173136.

Who is the listed applicant for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

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

What is the FDA product code for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses?

The FDA product code for Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses is MRC.

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Fonte oficial

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