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FDA 510(k)

Medline ReNewal 再生調和 ACE+7 剪刀

K 號:K193563 · 2020-08-19

決定日期2020-08-19
產品代碼NLQ
決定相當於

器材摘要

Medline ReNewal Reprocessed Harmonic ACE+7 Shears is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instrument Service and Savings Inc.(Dba Medline Ren. It received FDA 510(k) clearance on 2020-08-19 under 510(k) number K193563. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

常見問題

What is the Medline ReNewal Reprocessed Harmonic ACE+7 Shears?

Medline ReNewal Reprocessed Harmonic ACE+7 Shears is a medical device that received FDA 510(k) clearance on 2020-08-19. The listed applicant is Surgical Instrument Service and Savings Inc.(Dba Medline Ren. The 510(k) number is K193563.

When did Medline ReNewal Reprocessed Harmonic ACE+7 Shears receive FDA 510(k) clearance?

Medline ReNewal Reprocessed Harmonic ACE+7 Shears received FDA 510(k) clearance on 2020-08-19, under 510(k) number K193563.

Who is the listed applicant for Medline ReNewal Reprocessed Harmonic ACE+7 Shears?

The FDA 510(k) record lists Surgical Instrument Service and Savings Inc.(Dba Medline Ren as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline ReNewal Reprocessed Harmonic ACE+7 Shears?

The FDA product code for Medline ReNewal Reprocessed Harmonic ACE+7 Shears is NLQ.

相關臨床試驗

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其他以 Surgical Instrument Service and Savings Inc.(Dba Medline Ren 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:NLQ)

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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