FDA 510(k)

Storz Medical MAGNETOLITH 肌肉刺激器

K号: K203710 · 2021-05-03

决定日期2021-05-03

产品代码IPF

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决定实质等同

器械摘要

Storz Medical MAGNETOLITH Muscle Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Storz Medical AG. It received FDA 510(k) clearance on 2021-05-03 under 510(k) number K203710. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Storz Medical MAGNETOLITH Muscle Stimulator?

Storz Medical MAGNETOLITH Muscle Stimulator is a medical device that received FDA 510(k) clearance on 2021-05-03. The listed applicant is Storz Medical AG. The 510(k) number is K203710.

When did Storz Medical MAGNETOLITH Muscle Stimulator receive FDA 510(k) clearance?

Storz Medical MAGNETOLITH Muscle Stimulator received FDA 510(k) clearance on 2021-05-03, under 510(k) number K203710.

Who is the listed applicant for Storz Medical MAGNETOLITH Muscle Stimulator?

The FDA 510(k) record lists Storz Medical AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Storz Medical MAGNETOLITH Muscle Stimulator?

The FDA product code for Storz Medical MAGNETOLITH Muscle Stimulator is IPF.

列明Storz Medical AG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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官方来源

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