FDA 510(k)

Compound W Nitro-Freeze

K号: K172373 · 2017-11-02

决定日期2017-11-02

产品代码GEH

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决定实质等同

器械摘要

Compound W Nitro-Freeze is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products, Inc.. It received FDA 510(k) clearance on 2017-11-02 under 510(k) number K172373. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Compound W Nitro-Freeze?

Compound W Nitro-Freeze is a medical device that received FDA 510(k) clearance on 2017-11-02. The listed applicant is Medtech Products, Inc.. The 510(k) number is K172373.

When did Compound W Nitro-Freeze receive FDA 510(k) clearance?

Compound W Nitro-Freeze received FDA 510(k) clearance on 2017-11-02, under 510(k) number K172373.

Who is the listed applicant for Compound W Nitro-Freeze?

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

What is the FDA product code for Compound W Nitro-Freeze?

The FDA product code for Compound W Nitro-Freeze is GEH.

列明Medtech Products, 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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相关器械（代码：GEH）

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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