系統，雷射，心肌內血管重建
PMA 核准號：P970029 · 2022-09-01
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器材摘要
SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION is the device name listed in this FDA 510(k) record. The listed applicant is Cryolife, Inc.. It received FDA 510(k) clearance on 2022-09-01. The device is classified under product code MNO. It was reviewed by the CV advisory panel.
常見問題
What is the SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION?
SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION is a medical device that received FDA 510(k) clearance on 2022-09-01. The listed applicant is Cryolife, Inc..
When did SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION receive FDA 510(k) clearance?
The clearance date for SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION can be found in the official FDA records.
Who is the listed applicant for SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION?
The FDA 510(k) record lists Cryolife, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION?
The FDA product code for SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION is MNO.
相關臨床試驗
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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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