ENT BIOTECH SOLUTIONS 组织移除设备(ELASSO)
K号: K152702 · 2016-02-18
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器械摘要
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
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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。
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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