Shapiro MD型号激光272
K号: K193667 · 2020-03-25
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决定日期2020-03-25
产品代码OAP
咨询委员会PM
请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。
决定实质等同
器械摘要
Shapiro MD model laser 272 is the device name listed in this FDA 510(k) record. The listed applicant is Conversion Labs, Pr, LLC. It received FDA 510(k) clearance on 2020-03-25 under 510(k) number K193667. 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 Shapiro MD model laser 272?
Shapiro MD model laser 272 is a medical device that received FDA 510(k) clearance on 2020-03-25. The listed applicant is Conversion Labs, Pr, LLC. The 510(k) number is K193667.
When did Shapiro MD model laser 272 receive FDA 510(k) clearance?
Shapiro MD model laser 272 received FDA 510(k) clearance on 2020-03-25, under 510(k) number K193667.
Who is the listed applicant for Shapiro MD model laser 272?
The FDA 510(k) record lists Conversion Labs, Pr, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Shapiro MD model laser 272?
The FDA product code for Shapiro MD model laser 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。
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
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