FDA 510(k)

PEAK NS033CF, PEAK NS017CF

K号: K180565 · 2018-06-13

决定日期2018-06-13

产品代码ELW

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决定实质等同

器械摘要

PEAK NS033CF, PEAK NS017CF is the device name listed in this FDA 510(k) record. The listed applicant is Neosil Co., Ltd.. It received FDA 510(k) clearance on 2018-06-13 under 510(k) number K180565. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PEAK NS033CF, PEAK NS017CF?

PEAK NS033CF, PEAK NS017CF is a medical device that received FDA 510(k) clearance on 2018-06-13. The listed applicant is Neosil Co., Ltd.. The 510(k) number is K180565.

When did PEAK NS033CF, PEAK NS017CF receive FDA 510(k) clearance?

PEAK NS033CF, PEAK NS017CF received FDA 510(k) clearance on 2018-06-13, under 510(k) number K180565.

Who is the listed applicant for PEAK NS033CF, PEAK NS017CF?

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

What is the FDA product code for PEAK NS033CF, PEAK NS017CF?

The FDA product code for PEAK NS033CF, PEAK NS017CF is ELW.

相关器械（代码：ELW）

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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