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FDA 510(k)

ProPerformance 康復系統

K 號：K192252 · 2019-09-19

申請人Menlo Brands, LLC
決定日期2019-09-19
產品代碼IRP
諮詢委員會PM
決定相當於

器材摘要

ProPerformance Recovery System is the device name listed in this FDA 510(k) record. The listed applicant is Menlo Brands, LLC. It received FDA 510(k) clearance on 2019-09-19 under 510(k) number K192252. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ProPerformance Recovery System?

ProPerformance Recovery System is a medical device that received FDA 510(k) clearance on 2019-09-19. The listed applicant is Menlo Brands, LLC. The 510(k) number is K192252.

When did ProPerformance Recovery System receive FDA 510(k) clearance?

ProPerformance Recovery System received FDA 510(k) clearance on 2019-09-19, under 510(k) number K192252.

Who is the listed applicant for ProPerformance Recovery System?

The FDA 510(k) record lists Menlo Brands, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ProPerformance Recovery System?

The FDA product code for ProPerformance Recovery System is IRP.

相關臨床試驗

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相關器械（代碼：IRP）

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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