充气器50L FM134
K号: K153513 · 2016-03-04
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决定日期2016-03-04
产品代码HIF
咨询委员会OB
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决定实质等同
器械摘要
Insufflator 50L FM134 is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine GmbH. It received FDA 510(k) clearance on 2016-03-04 under 510(k) number K153513. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Insufflator 50L FM134?
Insufflator 50L FM134 is a medical device that received FDA 510(k) clearance on 2016-03-04. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K153513.
When did Insufflator 50L FM134 receive FDA 510(k) clearance?
Insufflator 50L FM134 received FDA 510(k) clearance on 2016-03-04, under 510(k) number K153513.
Who is the listed applicant for Insufflator 50L FM134?
The FDA 510(k) record lists W.O.M. World of Medicine GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Insufflator 50L FM134?
The FDA product code for Insufflator 50L FM134 is HIF.
相关临床试验
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列明W.O.M. World of Medicine 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：HIF）
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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