BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)
K号: K171404 · 2017-07-17
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器械摘要
常见问题
What is the BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)?
BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B) is a medical device that received FDA 510(k) clearance on 2017-07-17. The listed applicant is Bausch + Lomb, Incorporated. The 510(k) number is K171404.
When did BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B) receive FDA 510(k) clearance?
BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B) received FDA 510(k) clearance on 2017-07-17, under 510(k) number K171404.
Who is the listed applicant for BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)?
The FDA 510(k) record lists Bausch + Lomb, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)?
The FDA product code for BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B) is HQD.
相关临床试验
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。
列明Bausch + Lomb, Incorporated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:HQD)
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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