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FDA 510(k)

HydroMARK 乳癌切片位置標記器

K 號:K210752 · 2021-04-14

決定日期2021-04-14
產品代碼NEU
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

HydroMARK Breast Biopsy Site Marker is the device name listed in this FDA 510(k) record. The listed applicant is Devicor Medical Products, Inc.. It received FDA 510(k) clearance on 2021-04-14 under 510(k) number K210752. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the HydroMARK Breast Biopsy Site Marker?

HydroMARK Breast Biopsy Site Marker is a medical device that received FDA 510(k) clearance on 2021-04-14. The listed applicant is Devicor Medical Products, Inc.. The 510(k) number is K210752.

When did HydroMARK Breast Biopsy Site Marker receive FDA 510(k) clearance?

HydroMARK Breast Biopsy Site Marker received FDA 510(k) clearance on 2021-04-14, under 510(k) number K210752.

Who is the listed applicant for HydroMARK Breast Biopsy Site Marker?

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

What is the FDA product code for HydroMARK Breast Biopsy Site Marker?

The FDA product code for HydroMARK Breast Biopsy Site Marker is NEU.

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其他以 Devicor Medical Products, Inc. 為申請人之記錄

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相關器械(代碼:NEU)

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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