SuperGrow 272，Ultimate 272
K号: K172982 · 2017-12-19
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决定日期2017-12-19
产品代码OAP
咨询委员会PM
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决定实质等同
器械摘要
SuperGrow 272, Ultimate 272 is the device name listed in this FDA 510(k) record. The listed applicant is Super Grow Lasers. It received FDA 510(k) clearance on 2017-12-19 under 510(k) number K172982. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SuperGrow 272, Ultimate 272?
SuperGrow 272, Ultimate 272 is a medical device that received FDA 510(k) clearance on 2017-12-19. The listed applicant is Super Grow Lasers. The 510(k) number is K172982.
When did SuperGrow 272, Ultimate 272 receive FDA 510(k) clearance?
SuperGrow 272, Ultimate 272 received FDA 510(k) clearance on 2017-12-19, under 510(k) number K172982.
Who is the listed applicant for SuperGrow 272, Ultimate 272?
The FDA 510(k) record lists Super Grow Lasers as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SuperGrow 272, Ultimate 272?
The FDA product code for SuperGrow 272, Ultimate 272 is OAP.
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Super Grow Lasers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：OAP）
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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