SHUNT，门静脉，内支架
PMA编号：P250050 · 2026-09-25
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器械摘要
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.
常见问题
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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官方来源
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