FDA 510(k)

羅盤導向針

K 號：K221206 · 2022-08-25

決定日期2022-08-25

產品代碼KTI

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

Compass Steerable Needle is the device name listed in this FDA 510(k) record. The listed applicant is Serpex Medical, Inc.. It received FDA 510(k) clearance on 2022-08-25 under 510(k) number K221206. The device is classified under product code KTI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Compass Steerable Needle?

Compass Steerable Needle is a medical device that received FDA 510(k) clearance on 2022-08-25. The listed applicant is Serpex Medical, Inc.. The 510(k) number is K221206.

When did Compass Steerable Needle receive FDA 510(k) clearance?

Compass Steerable Needle received FDA 510(k) clearance on 2022-08-25, under 510(k) number K221206.

Who is the listed applicant for Compass Steerable Needle?

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

What is the FDA product code for Compass Steerable Needle?

The FDA product code for Compass Steerable Needle is KTI.

其他以 Serpex Medical, Inc. 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。

K252874羅盤可調針針與適配器 SRA-1-01 及 SRA-2-01 K221302Recon可調向套管

相關器械（代碼：KTI）

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。

K261274EchoTip Ultra® 高解析度內視鏡超聲針對 Fujifilm 鏡頭；EchoTip ProCore® 高解析度內視鏡超聲針對 Fujifilm 鏡頭Cook Ireland, Ltd.K251478ClearTip TBNA 型號Finemedix Co., Ltd.K254040肺流籃狀導管Free Flow Medical, Inc.K251402LIA-1 管針（542-1）Leadoptik, Inc.K252874羅盤可調針針與適配器 SRA-1-01 及 SRA-2-01Serpex Medical, Inc.K251664單次使用抽吸針 (NA-201SX-4021)；單次使用抽吸針 (NA-201SX-4022)Olympus Medical Systems Corporation

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。