FDA 510(k)

SuperNO2VA Et 设备

K号: K173147 · 2018-06-20

决定日期2018-06-20

产品代码CCK

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决定实质等同

器械摘要

SuperNO2VA Et Device is the device name listed in this FDA 510(k) record. The listed applicant is Revolutionary Medical Devices, Inc.. It received FDA 510(k) clearance on 2018-06-20 under 510(k) number K173147. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the SuperNO2VA Et Device?

SuperNO2VA Et Device is a medical device that received FDA 510(k) clearance on 2018-06-20. The listed applicant is Revolutionary Medical Devices, Inc.. The 510(k) number is K173147.

When did SuperNO2VA Et Device receive FDA 510(k) clearance?

SuperNO2VA Et Device received FDA 510(k) clearance on 2018-06-20, under 510(k) number K173147.

Who is the listed applicant for SuperNO2VA Et Device?

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

What is the FDA product code for SuperNO2VA Et Device?

The FDA product code for SuperNO2VA Et Device is CCK.

列明Revolutionary Medical Devices, 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。

K163277SuperNO2VA 设备

官方来源

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