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FDA 510(k)

Portex Blue Line Ultra 儿童气管切开管

K号: K170720 · 2017-12-07

决定日期2017-12-07
产品代码JOH
咨询委员会AN 请注意,由于您没有提供完整的医疗设备监管文本,我无法提供完整的翻译。如果您能提供完整的文本,我将很乐意为您翻译。
决定实质等同

器械摘要

Portex Blue Line Ultra Paediatric Tracheosomy Tube is the device name listed in this FDA 510(k) record. The listed applicant is Smiths Medical Asd, Inc.. It received FDA 510(k) clearance on 2017-12-07 under 510(k) number K170720. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Portex Blue Line Ultra Paediatric Tracheosomy Tube?

Portex Blue Line Ultra Paediatric Tracheosomy Tube is a medical device that received FDA 510(k) clearance on 2017-12-07. The listed applicant is Smiths Medical Asd, Inc.. The 510(k) number is K170720.

When did Portex Blue Line Ultra Paediatric Tracheosomy Tube receive FDA 510(k) clearance?

Portex Blue Line Ultra Paediatric Tracheosomy Tube received FDA 510(k) clearance on 2017-12-07, under 510(k) number K170720.

Who is the listed applicant for Portex Blue Line Ultra Paediatric Tracheosomy Tube?

The FDA 510(k) record lists Smiths Medical Asd, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Portex Blue Line Ultra Paediatric Tracheosomy Tube?

The FDA product code for Portex Blue Line Ultra Paediatric Tracheosomy Tube is JOH.

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列明Smiths Medical Asd, Inc.为申报人的其他记录

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相关器械(代码:JOH)

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

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