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FDA 510(k)

Cautery Protective Actuation System (CPAS)

K号: K232407 · 2023-10-06

决定日期2023-10-06
产品代码GEI
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决定实质等同

器械摘要

Cautery Protective Actuation System (CPAS) is the device name listed in this FDA 510(k) record. The listed applicant is Safer Surgeries Medical Devices, LLC. It received FDA 510(k) clearance on 2023-10-06 under 510(k) number K232407. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Cautery Protective Actuation System (CPAS)?

Cautery Protective Actuation System (CPAS) is a medical device that received FDA 510(k) clearance on 2023-10-06. The listed applicant is Safer Surgeries Medical Devices, LLC. The 510(k) number is K232407.

When did Cautery Protective Actuation System (CPAS) receive FDA 510(k) clearance?

Cautery Protective Actuation System (CPAS) received FDA 510(k) clearance on 2023-10-06, under 510(k) number K232407.

Who is the listed applicant for Cautery Protective Actuation System (CPAS)?

The FDA 510(k) record lists Safer Surgeries Medical Devices, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cautery Protective Actuation System (CPAS)?

The FDA product code for Cautery Protective Actuation System (CPAS) is GEI.

相关临床试验

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相关器械(代码:GEI)

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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