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FDA 510(k)

再處理HARMONIC ACE+ 7剪刀,配備先進止血功能

K 號:K182272 · 2019-04-15

決定日期2019-04-15
產品代碼NLQ
決定相當於

器材摘要

Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2019-04-15 under 510(k) number K182272. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

常見問題

What is the Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis?

Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis is a medical device that received FDA 510(k) clearance on 2019-04-15. The listed applicant is Sterilmed, Inc.. The 510(k) number is K182272.

When did Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis receive FDA 510(k) clearance?

Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis received FDA 510(k) clearance on 2019-04-15, under 510(k) number K182272.

Who is the listed applicant for Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis?

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

What is the FDA product code for Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis?

The FDA product code for Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis is NLQ.

相關臨床試驗

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其他以 Sterilmed, Inc. 為申請人之記錄

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相關器械(代碼:NLQ)

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官方來源

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