免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料，僅供一般參考，不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

CryoValve SG 肺動脈瓣 (SGPV10) CryoValve SG 肺動脈瓣及導管 (SGPV00)

K 號：K252059 · 2025-10-02

申請人Artivion, Inc.
決定日期2025-10-02
產品代碼OHA
決定相當於

器材摘要

CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00) is the device name listed in this FDA 510(k) record. The listed applicant is Artivion, Inc.. It received FDA 510(k) clearance on 2025-10-02 under 510(k) number K252059. The device is classified under product code OHA. FDA Decision: Substantially Equivalent.

常見問題

What is the CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00)?

CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00) is a medical device that received FDA 510(k) clearance on 2025-10-02. The listed applicant is Artivion, Inc.. The 510(k) number is K252059.

When did CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00) receive FDA 510(k) clearance?

CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00) received FDA 510(k) clearance on 2025-10-02, under 510(k) number K252059.

Who is the listed applicant for CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00)?

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

What is the FDA product code for CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00)?

The FDA product code for CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00) is OHA.

相關臨床試驗

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

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。

↑