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FDA 510(k)

Optixon 1-Day

K号: K201013 · 2020-09-18

申请人Optixon, Inc.
决定日期2020-09-18
产品代码LPL
咨询委员会OP 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

Optixon 1-Day is the device name listed in this FDA 510(k) record. The listed applicant is Optixon, Inc.. It received FDA 510(k) clearance on 2020-09-18 under 510(k) number K201013. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Optixon 1-Day?

Optixon 1-Day is a medical device that received FDA 510(k) clearance on 2020-09-18. The listed applicant is Optixon, Inc.. The 510(k) number is K201013.

When did Optixon 1-Day receive FDA 510(k) clearance?

Optixon 1-Day received FDA 510(k) clearance on 2020-09-18, under 510(k) number K201013.

Who is the listed applicant for Optixon 1-Day?

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

What is the FDA product code for Optixon 1-Day?

The FDA product code for Optixon 1-Day is LPL.

相关临床试验

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相关器械(代码:LPL)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

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