FDA 510(k)

PosiSep 耳部碎裂敷料

K 號：K210411 · 2022-05-05

決定日期2022-05-05

產品代碼NHB

諮詢委員會中文(台灣): 此醫療設備之規範性文件遵循「醫療規範-v1」政策。以下為該文件之翻譯：此醫療設備已通過美國食品藥品管理局（FDA）的510(k)認證，並獲得PMA許可。該設備的臨床試驗編號為NCTXXXXXXX，並在PubMed上以PMIDXXXXXXX登錄。該設備的識別碼為XXXXXXXX，相關資訊請參考以下網址：[URL]。公司名稱：[公司名稱] 產品名稱：[產品名稱]

決定相當於

器材摘要

PosiSep EAR Fragmentable Ear Dressing is the device name listed in this FDA 510(k) record. The listed applicant is Hemostasis, LLC. It received FDA 510(k) clearance on 2022-05-05 under 510(k) number K210411. The device is classified under product code NHB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the PosiSep EAR Fragmentable Ear Dressing?

PosiSep EAR Fragmentable Ear Dressing is a medical device that received FDA 510(k) clearance on 2022-05-05. The listed applicant is Hemostasis, LLC. The 510(k) number is K210411.

When did PosiSep EAR Fragmentable Ear Dressing receive FDA 510(k) clearance?

PosiSep EAR Fragmentable Ear Dressing received FDA 510(k) clearance on 2022-05-05, under 510(k) number K210411.

Who is the listed applicant for PosiSep EAR Fragmentable Ear Dressing?

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

What is the FDA product code for PosiSep EAR Fragmentable Ear Dressing?

The FDA product code for PosiSep EAR Fragmentable Ear Dressing is NHB.

其他以 Hemostasis, LLC 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。

K234131解決內視鏡止血系統 K220326PosiSep X BAM 止血敷料/鼻內支撐

相關器械（代碼：NHB）

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。

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官方來源

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