Propeller 系统
K号: K152882 · 2016-03-08
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决定日期2016-03-08
产品代码CAF
咨询委员会AN
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决定实质等同
器械摘要
Propeller System is the device name listed in this FDA 510(k) record. The listed applicant is Reciprocal Labs. It received FDA 510(k) clearance on 2016-03-08 under 510(k) number K152882. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Propeller System?
Propeller System is a medical device that received FDA 510(k) clearance on 2016-03-08. The listed applicant is Reciprocal Labs. The 510(k) number is K152882.
When did Propeller System receive FDA 510(k) clearance?
Propeller System received FDA 510(k) clearance on 2016-03-08, under 510(k) number K152882.
Who is the listed applicant for Propeller System?
The FDA 510(k) record lists Reciprocal Labs as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Propeller System?
The FDA product code for Propeller System is CAF.
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Reciprocal Labs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：CAF）
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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