FDA 510(k)

Medline通用接地垫

K号: K212093 · 2022-01-14

决定日期2022-01-14

产品代码GEI

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决定实质等同

器械摘要

Medline Universal Grounding Pad is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2022-01-14 under 510(k) number K212093. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Medline Universal Grounding Pad?

Medline Universal Grounding Pad is a medical device that received FDA 510(k) clearance on 2022-01-14. The listed applicant is Medline Industries, Inc.. The 510(k) number is K212093.

When did Medline Universal Grounding Pad receive FDA 510(k) clearance?

Medline Universal Grounding Pad received FDA 510(k) clearance on 2022-01-14, under 510(k) number K212093.

Who is the listed applicant for Medline Universal Grounding Pad?

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

What is the FDA product code for Medline Universal Grounding Pad?

The FDA product code for Medline Universal Grounding Pad is GEI.

列明Medline Industries, 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：GEI）

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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