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FDA 510(k)

Passy Muir 气管切开术病毒和细菌气道保护过滤器(PM-APF15)

K号: K230483 · 2023-09-16

决定日期2023-09-16
产品代码CAH
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

Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15) is the device name listed in this FDA 510(k) record. The listed applicant is Passy-Muir, Inc.. It received FDA 510(k) clearance on 2023-09-16 under 510(k) number K230483. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15)?

Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15) is a medical device that received FDA 510(k) clearance on 2023-09-16. The listed applicant is Passy-Muir, Inc.. The 510(k) number is K230483.

When did Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15) receive FDA 510(k) clearance?

Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15) received FDA 510(k) clearance on 2023-09-16, under 510(k) number K230483.

Who is the listed applicant for Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15)?

The FDA 510(k) record lists Passy-Muir, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15)?

The FDA product code for Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15) is CAH.

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。

相关器械(代码:CAH)

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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