FDA 510(k)

BAG手动复苏器和附件

K号: K251631 · 2025-11-24

决定日期2025-11-24

产品代码BTM

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决定实质等同

器械摘要

The BAG manual resuscitator and accessories is the device name listed in this FDA 510(k) record. The listed applicant is Laerdal Medical AS. It received FDA 510(k) clearance on 2025-11-24 under 510(k) number K251631. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the The BAG manual resuscitator and accessories?

The BAG manual resuscitator and accessories is a medical device that received FDA 510(k) clearance on 2025-11-24. The listed applicant is Laerdal Medical AS. The 510(k) number is K251631.

When did The BAG manual resuscitator and accessories receive FDA 510(k) clearance?

The BAG manual resuscitator and accessories received FDA 510(k) clearance on 2025-11-24, under 510(k) number K251631.

Who is the listed applicant for The BAG manual resuscitator and accessories?

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

What is the FDA product code for The BAG manual resuscitator and accessories?

The FDA product code for The BAG manual resuscitator and accessories is BTM.

列明Laerdal Medical AS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：BTM）

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。

K243861蝴蝶BVMCompact Medical, Inc.K221841EOlife®Archeon K212905Sotair 设备Safe Bvm Corporation K210288一次性手动复苏器Xiamen Compower Medical Tech. Co., Ltd.K181583成人一次性复苏器袋（不带压力释放），成人一次性复苏器袋+压力释放40CMH20，成人一次性复苏器袋+压力释放60CMH20，儿童一次性复苏器袋+压力释放40CMH20，婴儿一次性复苏器袋+压力释放40CMH20Flexicare Medical Limited.K170663Foremount 可弃用PVC复苏器，Foremount 可弃用PEEP 阀，Foremount 可弃用压力计Foremount Enterprise Co., Ltd.

官方来源

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