FDA 510(k)

RF1400 運動壓縮包

K 號：K162481 · 2017-02-16

決定日期2017-02-16

產品代碼JOW

諮詢委員會履歷

決定相當於

器材摘要

RF1400 Active Compression Wrap is the device name listed in this FDA 510(k) record. The listed applicant is Recovery Force, LLC. It received FDA 510(k) clearance on 2017-02-16 under 510(k) number K162481. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the RF1400 Active Compression Wrap?

RF1400 Active Compression Wrap is a medical device that received FDA 510(k) clearance on 2017-02-16. The listed applicant is Recovery Force, LLC. The 510(k) number is K162481.

When did RF1400 Active Compression Wrap receive FDA 510(k) clearance?

RF1400 Active Compression Wrap received FDA 510(k) clearance on 2017-02-16, under 510(k) number K162481.

Who is the listed applicant for RF1400 Active Compression Wrap?

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

What is the FDA product code for RF1400 Active Compression Wrap?

The FDA product code for RF1400 Active Compression Wrap is JOW.

其他以 Recovery Force, LLC 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。

K203052移動與壓縮系統（MAC系統）

相關器械（代碼：JOW）

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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