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FDA 510(k)

ENT BIOTECH SOLUTIONS 组织移除设备(ELASSO)

K号: K152702 · 2016-02-18

决定日期2016-02-18
产品代码GEI
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO) is the device name listed in this FDA 510(k) record. The listed applicant is Ent Biotech Solutions. It received FDA 510(k) clearance on 2016-02-18 under 510(k) number K152702. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO)?

ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO) is a medical device that received FDA 510(k) clearance on 2016-02-18. The listed applicant is Ent Biotech Solutions. The 510(k) number is K152702.

When did ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO) receive FDA 510(k) clearance?

ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO) received FDA 510(k) clearance on 2016-02-18, under 510(k) number K152702.

Who is the listed applicant for ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO)?

The FDA 510(k) record lists Ent Biotech Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO)?

The FDA product code for ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO) is GEI.

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。

相关器械(代码:GEI)

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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