Crystalsert 镜片输送系统
K号: K173480 · 2017-12-11
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决定日期2017-12-11
产品代码MSS
咨询委员会OP
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决定实质等同
器械摘要
Crystalsert Lens Delivery System is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 2017-12-11 under 510(k) number K173480. The device is classified under product code MSS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Crystalsert Lens Delivery System?
Crystalsert Lens Delivery System is a medical device that received FDA 510(k) clearance on 2017-12-11. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K173480.
When did Crystalsert Lens Delivery System receive FDA 510(k) clearance?
Crystalsert Lens Delivery System received FDA 510(k) clearance on 2017-12-11, under 510(k) number K173480.
Who is the listed applicant for Crystalsert Lens Delivery System?
The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Crystalsert Lens Delivery System?
The FDA product code for Crystalsert Lens Delivery System is MSS.
相关临床试验
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列明Bausch & Lomb, Inc.为申报人的其他记录
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。
相关器械（代码：MSS）
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。
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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