FDA 510(k)

模型 WP-3840 及 WP-3040

K 號：K173848 · 2018-08-07

決定日期2018-08-07

產品代碼IYE

諮詢委員會RA

決定相當於

器材摘要

Model WP-3840 and WP-3040 is the device name listed in this FDA 510(k) record. The listed applicant is Cnmc Co., Inc.. It received FDA 510(k) clearance on 2018-08-07 under 510(k) number K173848. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Model WP-3840 and WP-3040?

Model WP-3840 and WP-3040 is a medical device that received FDA 510(k) clearance on 2018-08-07. The listed applicant is Cnmc Co., Inc.. The 510(k) number is K173848.

When did Model WP-3840 and WP-3040 receive FDA 510(k) clearance?

Model WP-3840 and WP-3040 received FDA 510(k) clearance on 2018-08-07, under 510(k) number K173848.

Who is the listed applicant for Model WP-3840 and WP-3040?

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

What is the FDA product code for Model WP-3840 and WP-3040?

The FDA product code for Model WP-3840 and WP-3040 is IYE.

相關器械（代碼：IYE）

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：IYE）

官方來源