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FDA 510(k)

Airbile-100

K号: K250976 · 2025-12-19

决定日期2025-12-19
产品代码IZL
咨询委员会RA
决定实质等同

器械摘要

Airbile-100 is the device name listed in this FDA 510(k) record. The listed applicant is Poskom Co., Ltd.. It received FDA 510(k) clearance on 2025-12-19 under 510(k) number K250976. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Airbile-100?

Airbile-100 is a medical device that received FDA 510(k) clearance on 2025-12-19. The listed applicant is Poskom Co., Ltd.. The 510(k) number is K250976.

When did Airbile-100 receive FDA 510(k) clearance?

Airbile-100 received FDA 510(k) clearance on 2025-12-19, under 510(k) number K250976.

Who is the listed applicant for Airbile-100?

The FDA 510(k) record lists Poskom Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Airbile-100?

The FDA product code for Airbile-100 is IZL.

相关临床试验

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列明Poskom Co., Ltd.为申报人的其他记录

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相关器械(代码:IZL)

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官方来源

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