FDA 510(k)

Storz醫療MAGNETOLITH肌肉刺激器

K 號：K203710 · 2021-05-03

決定日期2021-05-03

產品代碼IPF

諮詢委員會PM

決定相當於

器材摘要

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.

常見問題

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.

其他以 Storz Medical AG 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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相關器械（代碼：IPF）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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