支架，冠狀
PMA 核准號：P110004 · 2020-04-09
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器材摘要
STENT, CORONARY is the device name listed in this FDA 510(k) record. The listed applicant is Medinol, Ltd.. It received FDA 510(k) clearance on 2020-04-09. The device is classified under product code MAF. It was reviewed by the CV advisory panel.
常見問題
What is the STENT, CORONARY?
STENT, CORONARY is a medical device that received FDA 510(k) clearance on 2020-04-09. The listed applicant is Medinol, Ltd..
When did STENT, CORONARY receive FDA 510(k) clearance?
The clearance date for STENT, CORONARY can be found in the official FDA records.
Who is the listed applicant for STENT, CORONARY?
The FDA 510(k) record lists Medinol, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STENT, CORONARY?
The FDA product code for STENT, CORONARY is MAF.
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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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