Pulmonary valve prosthesis percutaneously delivered
PMA番号：P200015 · 2026-09-23
広告
医療機器の概要
Pulmonary valve prosthesis percutaneously delivered is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Lifesciences, LLC. It received FDA 510(k) clearance on 2026-09-23. The device is classified under product code NPV. It was reviewed by the CV advisory panel.
よくある質問
What is the Pulmonary valve prosthesis percutaneously delivered?
Pulmonary valve prosthesis percutaneously delivered is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is Edwards Lifesciences, LLC.
When did Pulmonary valve prosthesis percutaneously delivered receive FDA 510(k) clearance?
The clearance date for Pulmonary valve prosthesis percutaneously delivered can be found in the official FDA records.
Who is the listed applicant for Pulmonary valve prosthesis percutaneously delivered?
The FDA 510(k) record lists Edwards Lifesciences, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pulmonary valve prosthesis percutaneously delivered?
The FDA product code for Pulmonary valve prosthesis percutaneously delivered is NPV.
関連する臨床試験
関連レコードは、名称、製品コード、その他のメタデータを使用して自動的にマッチングされます。マッチは検証された臨床的、科学的、企業的、または規制上の関係を確立するものではありません。リンクされた公式情報源をご確認ください。
NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751膀胱癌を診断するための人工知能（AI）アシストドのUro-Camカテーテル評価システムNOT_YET_RECRUITING
公式ソース
FDAデータベースで見る →データはFDA Open APIから取得しています。最新かつ権威ある情報については、常に公式レコードを参照してください。
広告