EasyMark Tissue Marker
K号: K183503 · 2019-10-17
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器械摘要
EasyMark Tissue Marker is the device name listed in this FDA 510(k) record. The listed applicant is Inrad, Inc.. It received FDA 510(k) clearance on 2019-10-17 under 510(k) number K183503. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the EasyMark Tissue Marker?
EasyMark Tissue Marker is a medical device that received FDA 510(k) clearance on 2019-10-17. The listed applicant is Inrad, Inc.. The 510(k) number is K183503.
When did EasyMark Tissue Marker receive FDA 510(k) clearance?
EasyMark Tissue Marker received FDA 510(k) clearance on 2019-10-17, under 510(k) number K183503.
Who is the listed applicant for EasyMark Tissue Marker?
The FDA 510(k) record lists Inrad, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EasyMark Tissue Marker?
The FDA product code for EasyMark Tissue Marker is NEU.
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Inrad, 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：NEU）
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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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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