SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS
PMA 核准號：P250050 · 2026-09-25
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器材摘要
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code MIR. It was reviewed by the CV advisory panel.
常見問題
What is the SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS?
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Bard Peripheral Vascular, Inc..
When did SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS receive FDA 510(k) clearance?
The clearance date for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS can be found in the official FDA records.
Who is the listed applicant for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS?
The FDA 510(k) record lists Bard Peripheral Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS?
The FDA product code for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is MIR.
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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。
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