Amsel 阻塞器设备
K号: K172479 · 2017-09-14
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器械摘要
Amsel Occluder Device is the device name listed in this FDA 510(k) record. The listed applicant is Amsel Medical. It received FDA 510(k) clearance on 2017-09-14 under 510(k) number K172479. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Amsel Occluder Device?
Amsel Occluder Device is a medical device that received FDA 510(k) clearance on 2017-09-14. The listed applicant is Amsel Medical. The 510(k) number is K172479.
When did Amsel Occluder Device receive FDA 510(k) clearance?
Amsel Occluder Device received FDA 510(k) clearance on 2017-09-14, under 510(k) number K172479.
Who is the listed applicant for Amsel Occluder Device?
The FDA 510(k) record lists Amsel Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Amsel Occluder Device?
The FDA product code for Amsel Occluder Device is FZP.
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相关器械（代码：FZP）
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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