FDA 510(k)

AEON ȡ

K号: K180114 · 2018-03-27

决定日期2018-03-27

产品代码GCJ

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决定实质等同

器械摘要

AEON Retrieval Bag is the device name listed in this FDA 510(k) record. The listed applicant is Lexington Medical, Inc.. It received FDA 510(k) clearance on 2018-03-27 under 510(k) number K180114. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AEON Retrieval Bag?

AEON Retrieval Bag is a medical device that received FDA 510(k) clearance on 2018-03-27. The listed applicant is Lexington Medical, Inc.. The 510(k) number is K180114.

When did AEON Retrieval Bag receive FDA 510(k) clearance?

AEON Retrieval Bag received FDA 510(k) clearance on 2018-03-27, under 510(k) number K180114.

Who is the listed applicant for AEON Retrieval Bag?

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

What is the FDA product code for AEON Retrieval Bag?

The FDA product code for AEON Retrieval Bag is GCJ.

列明Lexington Medical, Inc.为申报人的其他记录

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。

K251482AEON™ ˿K234039AEON 内窥镜动力钉合器（短/AEPH060）；AEON 内窥镜动力钉合器（中/AEPH160）；AEON 内窥镜动力钉合器（长/AEPH260）K222210AEON 内窥镜钉合器 K201882AEON 内窥镜钉合器 K192235AEON 腹腔镜器械 K182380AEON 内窥镜钉合器

查看所有 9 个设备 →

相关器械（代码：GCJ）

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。

K262397CuratOR EX2742Eizo Corporation K260884UNIDRIVE选择系统Karl Storz SE & CO. KG K260972OEV-271MUH 液晶显示器；OEV-321MUH 液晶显示器；OEV-431MUH 液晶显示器Sony Corporation K261139VereSee（VER150、VER200、VER151、VER201、VER200C和VER-100-103）Freyja Healthcare, LLC K253541EZ-Close™（EZ Close 端口部位闭合装置，EZ Close MAX 端口部位闭合装置，EZ Close II 端口部位闭合装置）Medical Impact K261614LED液晶显示器（OEV-271H）Lg Electronics.Inc

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