Rapid HB，Rapid LB，Rapid MB
K号: K173318 · 2017-10-31
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决定日期2017-10-31
产品代码ELW
咨询委员会DE
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决定实质等同
器械摘要
Rapid HB, Rapid LB, Rapid MB is the device name listed in this FDA 510(k) record. The listed applicant is 3M Deutschland GmbH. It received FDA 510(k) clearance on 2017-10-31 under 510(k) number K173318. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Rapid HB, Rapid LB, Rapid MB?
Rapid HB, Rapid LB, Rapid MB is a medical device that received FDA 510(k) clearance on 2017-10-31. The listed applicant is 3M Deutschland GmbH. The 510(k) number is K173318.
When did Rapid HB, Rapid LB, Rapid MB receive FDA 510(k) clearance?
Rapid HB, Rapid LB, Rapid MB received FDA 510(k) clearance on 2017-10-31, under 510(k) number K173318.
Who is the listed applicant for Rapid HB, Rapid LB, Rapid MB?
The FDA 510(k) record lists 3M Deutschland GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Rapid HB, Rapid LB, Rapid MB?
The FDA product code for Rapid HB, Rapid LB, Rapid MB is ELW.
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3M Deutschland GmbH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：ELW）
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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