FDA 510(k)

Pekkton Ivory

K号: K170102 · 2017-11-13

决定日期2017-11-13

产品代码EBF

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决定实质等同

器械摘要

Pekkton Ivory is the device name listed in this FDA 510(k) record. The listed applicant is Cendres+Metaux SA. It received FDA 510(k) clearance on 2017-11-13 under 510(k) number K170102. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Pekkton Ivory?

Pekkton Ivory is a medical device that received FDA 510(k) clearance on 2017-11-13. The listed applicant is Cendres+Metaux SA. The 510(k) number is K170102.

When did Pekkton Ivory receive FDA 510(k) clearance?

Pekkton Ivory received FDA 510(k) clearance on 2017-11-13, under 510(k) number K170102.

Who is the listed applicant for Pekkton Ivory?

The FDA 510(k) record lists Cendres+Metaux SA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pekkton Ivory?

The FDA product code for Pekkton Ivory is EBF.

列明Cendres+Metaux SA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。

K192251Livento Press, Soprano 10, Soprano

官方来源

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