FDA 510(k)

BiopSee，移動美國

K 號：K170841 · 2017-07-26

決定日期2017-07-26

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

BiopSee, Mobile US is the device name listed in this FDA 510(k) record. The listed applicant is Medcom GmbH. It received FDA 510(k) clearance on 2017-07-26 under 510(k) number K170841. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BiopSee, Mobile US?

BiopSee, Mobile US is a medical device that received FDA 510(k) clearance on 2017-07-26. The listed applicant is Medcom GmbH. The 510(k) number is K170841.

When did BiopSee, Mobile US receive FDA 510(k) clearance?

BiopSee, Mobile US received FDA 510(k) clearance on 2017-07-26, under 510(k) number K170841.

Who is the listed applicant for BiopSee, Mobile US?

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

What is the FDA product code for BiopSee, Mobile US?

The FDA product code for BiopSee, Mobile US is LLZ.

其他以 Medcom GmbH 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。

K181789VeriSuite K180308預言 K163119NaviSuite SSI 版本

相關器械（代碼：LLZ）

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。

K261874Syneris PACS v.1.0.1.0Syneris K262442HipStudio分析Replasia BV K261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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。