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FDA 510(k)

Pantheris 管針(8F);Pantheris 管針(7F);Lightbox HS 影像控制台;Lightbox Sled

K 號:K163264 · 2016-12-21

申請人Avinger, Inc.
決定日期2016-12-21
產品代碼MCW
諮詢委員會履歷
決定相當於

器材摘要

Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled is the device name listed in this FDA 510(k) record. The listed applicant is Avinger, Inc.. It received FDA 510(k) clearance on 2016-12-21 under 510(k) number K163264. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled?

Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled is a medical device that received FDA 510(k) clearance on 2016-12-21. The listed applicant is Avinger, Inc.. The 510(k) number is K163264.

When did Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled receive FDA 510(k) clearance?

Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled received FDA 510(k) clearance on 2016-12-21, under 510(k) number K163264.

Who is the listed applicant for Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled?

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

What is the FDA product code for Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled?

The FDA product code for Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled is MCW.

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其他以 Avinger, Inc. 為申請人之記錄

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相關器械(代碼:MCW)

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。

官方來源

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