橫斷式乳攝影X光系統
PMA 核准號：P130025 · 2023-10-12
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器材摘要
Cross-sectional mammographic xray system is the device name listed in this FDA 510(k) record. The listed applicant is Koning Corporation. It received FDA 510(k) clearance on 2023-10-12. The device is classified under product code OLQ. It was reviewed by the RA advisory panel.
常見問題
What is the Cross-sectional mammographic xray system?
Cross-sectional mammographic xray system is a medical device that received FDA 510(k) clearance on 2023-10-12. The listed applicant is Koning Corporation.
When did Cross-sectional mammographic xray system receive FDA 510(k) clearance?
The clearance date for Cross-sectional mammographic xray system can be found in the official FDA records.
Who is the listed applicant for Cross-sectional mammographic xray system?
The FDA 510(k) record lists Koning Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cross-sectional mammographic xray system?
The FDA product code for Cross-sectional mammographic xray system is OLQ.
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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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