PNEUMOCLEAR
K号: K170784 · 2017-05-15
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决定日期2017-05-15
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
PNEUMOCLEAR 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 2017-05-15 under 510(k) number K170784. 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 PNEUMOCLEAR?
PNEUMOCLEAR is a medical device that received FDA 510(k) clearance on 2017-05-15. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K170784.
When did PNEUMOCLEAR receive FDA 510(k) clearance?
PNEUMOCLEAR received FDA 510(k) clearance on 2017-05-15, under 510(k) number K170784.
Who is the listed applicant for PNEUMOCLEAR?
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 PNEUMOCLEAR?
The FDA product code for PNEUMOCLEAR is HIF.
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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