藥物涂層週邊經皮腔內血管成形術導管
PMA 核准號：P190008 · 2026-05-21
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器材摘要
Drug-coated peripheral transluminal angioplasty catheter is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular, Inc.. It received FDA 510(k) clearance on 2026-05-21. The device is classified under product code PRC. It was reviewed by the CV advisory panel.
常見問題
What is the Drug-coated peripheral transluminal angioplasty catheter?
Drug-coated peripheral transluminal angioplasty catheter is a medical device that received FDA 510(k) clearance on 2026-05-21. The listed applicant is Medtronic Vascular, Inc..
When did Drug-coated peripheral transluminal angioplasty catheter receive FDA 510(k) clearance?
The clearance date for Drug-coated peripheral transluminal angioplasty catheter can be found in the official FDA records.
Who is the listed applicant for Drug-coated peripheral transluminal angioplasty catheter?
The FDA 510(k) record lists Medtronic Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Drug-coated peripheral transluminal angioplasty catheter?
The FDA product code for Drug-coated peripheral transluminal angioplasty catheter is PRC.
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官方來源
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