大動脈弁、移植用弁、皮膚内経由
PMA番号：P100041 · 2016-03-22
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医療機器の概要
Aortic 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 2016-03-22. The device is classified under product code NPT. It was reviewed by the CV advisory panel.
よくある質問
What is the Aortic valve, prosthesis, percutaneously delivered?
Aortic valve, prosthesis, percutaneously delivered is a medical device that received FDA 510(k) clearance on 2016-03-22. The listed applicant is Edwards Lifesciences, LLC.
When did Aortic valve, prosthesis, percutaneously delivered receive FDA 510(k) clearance?
The clearance date for Aortic valve, prosthesis, percutaneously delivered can be found in the official FDA records.
Who is the listed applicant for Aortic 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 Aortic valve, prosthesis, percutaneously delivered?
The FDA product code for Aortic valve, prosthesis, percutaneously delivered is NPT.
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。
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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。
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