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FDA 510(k)

ERBEFLO 2 内窥镜快速连接宾得镜头端口连接器

K号: K191438 · 2019-06-27

决定日期2019-06-27
产品代码OCX
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

ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector is the device name listed in this FDA 510(k) record. The listed applicant is Erbe USA, Inc.. It received FDA 510(k) clearance on 2019-06-27 under 510(k) number K191438. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector?

ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector is a medical device that received FDA 510(k) clearance on 2019-06-27. The listed applicant is Erbe USA, Inc.. The 510(k) number is K191438.

When did ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector receive FDA 510(k) clearance?

ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector received FDA 510(k) clearance on 2019-06-27, under 510(k) number K191438.

Who is the listed applicant for ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector?

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

What is the FDA product code for ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector?

The FDA product code for ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector is OCX.

相关临床试验

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列明Erbe USA, Inc.为申报人的其他记录

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相关器械(代码:OCX)

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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