FDA 510(k)

單次使用細針穿刺活檢（FNB）設備（NA-U210H）

K 號：K252646 · 2025-10-24

決定日期2025-10-24

產品代碼FCG

諮詢委員會GU

決定相當於

器材摘要

Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2025-10-24 under 510(k) number K252646. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)?

Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) is a medical device that received FDA 510(k) clearance on 2025-10-24. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K252646.

When did Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) receive FDA 510(k) clearance?

Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) received FDA 510(k) clearance on 2025-10-24, under 510(k) number K252646.

Who is the listed applicant for Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)?

FDA 510(k) 記錄將Olympus Medical Systems Corp. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)?

The FDA product code for Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) is FCG.

其他以 Olympus Medical Systems Corp. 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。

K2620794K攝影鏡頭 OLYMPUS CH-S700-08-LB 医療設備規範文本 K254056THUNDERBEAT 5 mm, 45 cm, 前動握把型 S (TB-0545FCS)；THUNDERBEAT 5 mm, 35 cm, 前動握把型 S (TB-0535FCS)；THUNDERBEAT 5 mm, 20 cm, 前動握把型 S (TB-0520FCS)K260580單次使用可重裝夾釘應用器（HX-810LR，HX-810UR）；夾釘（HX-610-090，HX-610-135）；長夾釘（HX-610-090L，HX-610-135L）；短夾釘（HX-610-090S，HX-610-135S）；超短夾釘（HX-610-135XS）K252341EVIS EXERA III 支气管內視鏡 (OLYMPUS BF-Q190)；EVIS EXERA III 支气管內視鏡 (OLYMPUS BF-H190)；EVIS EXERA III 支气管內視鏡 (OLYMPUS BF-1TH190)K251807單次使用電外科止血鉗 FD-410LR, FD-411UR, FD-412LR K253646單次使用遠端蓋 MAJ-2315 (MAJ-2315)

查看所有 80 項裝置 →

相關器械（代碼：FCG）

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。

K250994ClearTip FNA及FNB型別Finemedix Co., Ltd.K241209EchoTip AcuCore™ EUS 結締針 (ECHO-BX-19)Cook Ireland, Ltd.K231422精準胃腸內科設備Limaca Medical, Ltd.K231267清針Finemedix Co., Ltd.K230909EchoTip® AcuCore™ 超聲波針吸針 (ECHO-BX-3-22)Cook Ireland, Ltd.K212423EndoDrill® 型號 XBibbinstruments AB

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。