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FDA 510(k)

安全針刺器

K 號:K210328 · 2021-03-05

決定日期2021-03-05
產品代碼DRC
諮詢委員會履歷
決定相當於

器材摘要

SafeSept Blunt Needle is the device name listed in this FDA 510(k) record. The listed applicant is Pressure Products Medical Device Manufacturing, LLC. It received FDA 510(k) clearance on 2021-03-05 under 510(k) number K210328. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SafeSept Blunt Needle?

SafeSept Blunt Needle is a medical device that received FDA 510(k) clearance on 2021-03-05. The listed applicant is Pressure Products Medical Device Manufacturing, LLC. The 510(k) number is K210328.

When did SafeSept Blunt Needle receive FDA 510(k) clearance?

SafeSept Blunt Needle received FDA 510(k) clearance on 2021-03-05, under 510(k) number K210328.

Who is the listed applicant for SafeSept Blunt Needle?

The FDA 510(k) record lists Pressure Products Medical Device Manufacturing, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SafeSept Blunt Needle?

The FDA product code for SafeSept Blunt Needle is DRC.

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其他以 Pressure Products Medical Device Manufacturing, LLC 為申請人之記錄

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相關器械(代碼:DRC)

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官方來源

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