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FDA 510(k)

PENTAX 医疗 EPK-i7010 视频处理器带 EB 系列内镜

K号: K173679 · 2018-07-03

决定日期2018-07-03
产品代码PEA
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定实质等同

器械摘要

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is the device name listed in this FDA 510(k) record. The listed applicant is Pentax of America, Inc.. It received FDA 510(k) clearance on 2018-07-03 under 510(k) number K173679. The device is classified under product code PEA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is a medical device that received FDA 510(k) clearance on 2018-07-03. The listed applicant is Pentax of America, Inc.. The 510(k) number is K173679.

When did PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes receive FDA 510(k) clearance?

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes received FDA 510(k) clearance on 2018-07-03, under 510(k) number K173679.

Who is the listed applicant for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?

The FDA 510(k) record lists Pentax of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?

The FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is PEA.

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列明Pentax of America, Inc.为申报人的其他记录

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相关器械(代码:PEA)

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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