FDA 510(k)

Relieva Scout 多窦道扩张系统

K号: K153341 · 2016-02-12

决定日期2016-02-12

产品代码LRC

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决定实质等同

器械摘要

Relieva Scout Multi-Sinus Dilation System is the device name listed in this FDA 510(k) record. The listed applicant is Acclarent, Inc.. It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K153341. The device is classified under product code LRC. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Relieva Scout Multi-Sinus Dilation System?

Relieva Scout Multi-Sinus Dilation System is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Acclarent, Inc.. The 510(k) number is K153341.

When did Relieva Scout Multi-Sinus Dilation System receive FDA 510(k) clearance?

Relieva Scout Multi-Sinus Dilation System received FDA 510(k) clearance on 2016-02-12, under 510(k) number K153341.

Who is the listed applicant for Relieva Scout Multi-Sinus Dilation System?

The FDA 510(k) record lists Acclarent, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Relieva Scout Multi-Sinus Dilation System?

The FDA product code for Relieva Scout Multi-Sinus Dilation System is LRC.

列明Acclarent, 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。

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官方来源

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