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FDA 510(k)

膠珠(600-800微米)- 1毫升球體體積,膠珠(600-800微米)- 2毫升球體體積

K 號:K173891 · 2018-01-19

決定日期2018-01-19
產品代碼KRD
諮詢委員會履歷
決定相當於

器材摘要

Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2018-01-19 under 510(k) number K173891. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume?

Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume is a medical device that received FDA 510(k) clearance on 2018-01-19. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K173891.

When did Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume receive FDA 510(k) clearance?

Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume received FDA 510(k) clearance on 2018-01-19, under 510(k) number K173891.

Who is the listed applicant for Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume?

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

What is the FDA product code for Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume?

The FDA product code for Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume is KRD.

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其他以 Vascular Solutions, Inc. 為申請人之記錄

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相關器械(代碼:KRD)

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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