MaxiTears 接触镜 PF
K号: K182984 · 2019-07-24
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决定日期2019-07-24
产品代码MRC
咨询委员会OP
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决定实质等同
器械摘要
MaxiTears Contacts PF is the device name listed in this FDA 510(k) record. The listed applicant is Omnivision AG. It received FDA 510(k) clearance on 2019-07-24 under 510(k) number K182984. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MaxiTears Contacts PF?
MaxiTears Contacts PF is a medical device that received FDA 510(k) clearance on 2019-07-24. The listed applicant is Omnivision AG. The 510(k) number is K182984.
When did MaxiTears Contacts PF receive FDA 510(k) clearance?
MaxiTears Contacts PF received FDA 510(k) clearance on 2019-07-24, under 510(k) number K182984.
Who is the listed applicant for MaxiTears Contacts PF?
The FDA 510(k) record lists Omnivision AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MaxiTears Contacts PF?
The FDA product code for MaxiTears Contacts PF is MRC.
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相关器械（代码：MRC）
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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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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