Quickie® Q700-UP M
K号: K172384 · 2018-01-16
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决定日期2018-01-16
产品代码IPL
咨询委员会PM
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决定实质等同
器械摘要
Quickie(r) Q700-UP M is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical (Us), LLC. It received FDA 510(k) clearance on 2018-01-16 under 510(k) number K172384. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Quickie(r) Q700-UP M?
Quickie(r) Q700-UP M is a medical device that received FDA 510(k) clearance on 2018-01-16. The listed applicant is Sunrise Medical (Us), LLC. The 510(k) number is K172384.
When did Quickie(r) Q700-UP M receive FDA 510(k) clearance?
Quickie(r) Q700-UP M received FDA 510(k) clearance on 2018-01-16, under 510(k) number K172384.
Who is the listed applicant for Quickie(r) Q700-UP M?
The FDA 510(k) record lists Sunrise Medical (Us), LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Quickie(r) Q700-UP M?
The FDA product code for Quickie(r) Q700-UP M is IPL.
相关临床试验
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列明Sunrise Medical (Us), LLC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：IPL）
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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