FDA 510(k)

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses

Número K: K241398 · 2024-10-22

RequerenteTianjin Mastervision Technology Co., Ltd.

Data da decisão2024-10-22

Código do produtoHQD

Comité consultivoOP

DecisãoSubstantially Equivalent

Resumo do dispositivo

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin Mastervision Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-10-22 under 510(k) number K241398. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses?

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses is a medical device that received FDA 510(k) clearance on 2024-10-22. The listed applicant is Tianjin Mastervision Technology Co., Ltd.. The 510(k) number is K241398.

When did SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses receive FDA 510(k) clearance?

SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses received FDA 510(k) clearance on 2024-10-22, under 510(k) number K241398.

Who is the listed applicant for SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses?

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

What is the FDA product code for SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses?

The FDA product code for SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact Lenses is HQD.

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Dispositivos Relacionados (Código: HQD)

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