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FDA 510(k)

Megadyne足开关

K号: K191328 · 2019-07-26

决定日期2019-07-26
产品代码FYD
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决定实质等同

器械摘要

Megadyne Foot Switch is the device name listed in this FDA 510(k) record. The listed applicant is Megadyne Medical Products, Inc.. It received FDA 510(k) clearance on 2019-07-26 under 510(k) number K191328. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Megadyne Foot Switch?

Megadyne Foot Switch is a medical device that received FDA 510(k) clearance on 2019-07-26. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K191328.

When did Megadyne Foot Switch receive FDA 510(k) clearance?

Megadyne Foot Switch received FDA 510(k) clearance on 2019-07-26, under 510(k) number K191328.

Who is the listed applicant for Megadyne Foot Switch?

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

What is the FDA product code for Megadyne Foot Switch?

The FDA product code for Megadyne Foot Switch is FYD.

相关临床试验

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列明Megadyne Medical 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。

相关器械(代码:FYD)

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。

官方来源

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