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FDA 510(k)

Sleepnet Arie 全脸通风口罩;Sleepnet Arie 鼻通风口罩

K号: K251847 · 2026-01-15

决定日期2026-01-15
产品代码BZD
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

Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask is the device name listed in this FDA 510(k) record. The listed applicant is Sleepnet Corporation. It received FDA 510(k) clearance on 2026-01-15 under 510(k) number K251847. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask?

Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask is a medical device that received FDA 510(k) clearance on 2026-01-15. The listed applicant is Sleepnet Corporation. The 510(k) number is K251847.

When did Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask receive FDA 510(k) clearance?

Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask received FDA 510(k) clearance on 2026-01-15, under 510(k) number K251847.

Who is the listed applicant for Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask?

The FDA 510(k) record lists Sleepnet Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask?

The FDA product code for Sleepnet Arie Full Face Vented Mask; Sleepnet Arie Nasal Vented Mask is BZD.

相关临床试验

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列明Sleepnet Corporation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。

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相关器械(代码:BZD)

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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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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