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FDA 510(k)

一次性標本回收袋

K 號:K201243 · 2020-07-10

決定日期2020-07-10
產品代碼GCJ
諮詢委員會GU
決定相當於

器材摘要

Disposable Specimen Retrieval Bag is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Biosis Healing Biolog Ical Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-07-10 under 510(k) number K201243. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Disposable Specimen Retrieval Bag?

Disposable Specimen Retrieval Bag is a medical device that received FDA 510(k) clearance on 2020-07-10. The listed applicant is Beijing Biosis Healing Biolog Ical Technology Co., Ltd.. The 510(k) number is K201243.

When did Disposable Specimen Retrieval Bag receive FDA 510(k) clearance?

Disposable Specimen Retrieval Bag received FDA 510(k) clearance on 2020-07-10, under 510(k) number K201243.

Who is the listed applicant for Disposable Specimen Retrieval Bag?

The FDA 510(k) record lists Beijing Biosis Healing Biolog Ical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Specimen Retrieval Bag?

The FDA product code for Disposable Specimen Retrieval Bag is GCJ.

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其他以 Beijing Biosis Healing Biolog Ical Technology Co., Ltd. 為申請人之記錄

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相關器械(代碼:GCJ)

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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