FDA 510(k)

F5 體質 VS

K 號：K191874 · 2019-10-25

決定日期2019-10-25

產品代碼IPL

諮詢委員會PM

決定相當於

器材摘要

F5 Corpus VS is the device name listed in this FDA 510(k) record. The listed applicant is Permobil AB. It received FDA 510(k) clearance on 2019-10-25 under 510(k) number K191874. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the F5 Corpus VS?

F5 Corpus VS is a medical device that received FDA 510(k) clearance on 2019-10-25. The listed applicant is Permobil AB. The 510(k) number is K191874.

When did F5 Corpus VS receive FDA 510(k) clearance?

F5 Corpus VS received FDA 510(k) clearance on 2019-10-25, under 510(k) number K191874.

Who is the listed applicant for F5 Corpus VS?

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

What is the FDA product code for F5 Corpus VS?

The FDA product code for F5 Corpus VS is IPL.

其他以 Permobil AB 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。

K190682探索者迷你

相關器械（代碼：IPL）

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。

K243783步行復健訓練電動輪椅（ZW518）Shenzhen Zuowei Technology Co., Ltd.K202728Action Trackchair HawkAction Manufacturing, Inc.K203761ParaMotionPowerbasetec GmbH K191334泰克RMD（泰克機械化移動設備）TEKRMD02，TEKRMD03，TEKRMD04，TEKRMD04，TEKRMD05，TEKRMD06，TEKRMD07，TEKRMD08Matia Robotics (Us), Inc.K190682探索者迷你Permobil AB K182257UPnRIDEUpnride Robotics , Ltd.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。