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FDA 510(k)

ComASP Cefiderocol 0.008-128

K号: K230479 · 2023-05-18

决定日期2023-05-18
产品代码JWY
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器械摘要

ComASP Cefiderocol 0.008-128 is the device name listed in this FDA 510(k) record. The listed applicant is Liofilchem s.r.l.. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K230479. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ComASP Cefiderocol 0.008-128?

ComASP Cefiderocol 0.008-128 is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Liofilchem s.r.l.. The 510(k) number is K230479.

When did ComASP Cefiderocol 0.008-128 receive FDA 510(k) clearance?

ComASP Cefiderocol 0.008-128 received FDA 510(k) clearance on 2023-05-18, under 510(k) number K230479.

Who is the listed applicant for ComASP Cefiderocol 0.008-128?

The FDA 510(k) record lists Liofilchem s.r.l. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ComASP Cefiderocol 0.008-128?

The FDA product code for ComASP Cefiderocol 0.008-128 is JWY.

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列明Liofilchem s.r.l.为申报人的其他记录

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相关器械(代码:JWY)

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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