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FDA 510(k)

RELI 安全血液採集管固定器,RELI 血液採集管固定器

K 號:K173279 · 2018-05-14

決定日期2018-05-14
產品代碼FMI
諮詢委員會醫療設備規範文本翻譯如下: HO 注意:原文中未提供具體的醫療設備規範文本,因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於

器材摘要

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder is the device name listed in this FDA 510(k) record. The listed applicant is Myco Medical Supplies, Inc.. It received FDA 510(k) clearance on 2018-05-14 under 510(k) number K173279. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder?

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder is a medical device that received FDA 510(k) clearance on 2018-05-14. The listed applicant is Myco Medical Supplies, Inc.. The 510(k) number is K173279.

When did RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder receive FDA 510(k) clearance?

RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder received FDA 510(k) clearance on 2018-05-14, under 510(k) number K173279.

Who is the listed applicant for RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder?

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

What is the FDA product code for RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder?

The FDA product code for RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder is FMI.

相關臨床試驗

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其他以 Myco Medical Supplies, Inc. 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。

相關器械(代碼:FMI)

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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