Reliance Solo 消毒包装,Reliance Tandem 消毒包装
K号: K171533 · 2017-06-29
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器械摘要
常见问题
What is the Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap?
Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap is a medical device that received FDA 510(k) clearance on 2017-06-29. The listed applicant is Ahlstrom Nonwovens, LLC. The 510(k) number is K171533.
When did Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap receive FDA 510(k) clearance?
Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap received FDA 510(k) clearance on 2017-06-29, under 510(k) number K171533.
Who is the listed applicant for Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap?
The FDA 510(k) record lists Ahlstrom Nonwovens, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap?
The FDA product code for Reliance Solo Sterilization Wrap, Reliance Tandem Sterilization Wrap is FRG.
相关临床试验
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列明Ahlstrom Nonwovens, 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:FRG)
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。
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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