FDA 510(k)

生物優質雙極起搏電極导管

K 號：K242863 · 2025-06-15

決定日期2025-06-15

產品代碼LDF

諮詢委員會履歷

決定相當於

器材摘要

Bioptimal Bipolar Pacing Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Bioptimal International Pte. , Ltd.. It received FDA 510(k) clearance on 2025-06-15 under 510(k) number K242863. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bioptimal Bipolar Pacing Catheter?

Bioptimal Bipolar Pacing Catheter is a medical device that received FDA 510(k) clearance on 2025-06-15. The listed applicant is Bioptimal International Pte. , Ltd.. The 510(k) number is K242863.

When did Bioptimal Bipolar Pacing Catheter receive FDA 510(k) clearance?

Bioptimal Bipolar Pacing Catheter received FDA 510(k) clearance on 2025-06-15, under 510(k) number K242863.

Who is the listed applicant for Bioptimal Bipolar Pacing Catheter?

The FDA 510(k) record lists Bioptimal International Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bioptimal Bipolar Pacing Catheter?

The FDA product code for Bioptimal Bipolar Pacing Catheter is LDF.

其他以 Bioptimal International Pte. , Ltd. 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。

K252702生物優質肺動脈監測導管（TD2502NF、TD2502NGF、TD2502NDF、TD2502NCF、TD2502NCGF、TD2502NDGF、TD2502NDCF、TD2502NDCGF、TD2502NXCF、TD2502NDXF、TD2502NXCGF、TD2502NDXGF、TD2502NDXCF、TD2502NDXCGF、TD2502-110NF、TD2502-110NGF、TD2502-110NDF、TD2502-110NCF、TD2502-110NDGF、TD2502-110NDCF、TD2502-110NCGF、TD2502-110NDCGF、TD2502-110NXF、TD2502-110NXGF、TD2502-110NDXF、TD2502-110NXCF、TD2502-110NDXGF、TD2502-110NDXCF，TD2502-110NXCGF，TD2502-110NDXCGF，TD2602NF，TD2602N）

相關器械（代碼：LDF）

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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