AEON 内窥镜钉合器
K号: K173443 · 2018-02-01
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器械摘要
常见问题
What is the AEON Endoscopic Stapler?
AEON Endoscopic Stapler is a medical device that received FDA 510(k) clearance on 2018-02-01. The listed applicant is Lexington Medical, Inc.. The 510(k) number is K173443.
When did AEON Endoscopic Stapler receive FDA 510(k) clearance?
AEON Endoscopic Stapler received FDA 510(k) clearance on 2018-02-01, under 510(k) number K173443.
Who is the listed applicant for AEON Endoscopic Stapler?
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 Endoscopic Stapler?
The FDA product code for AEON Endoscopic Stapler is GDW.
相关临床试验
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。
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。
相关器械(代码:GDW)
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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