横截面乳腺摄影X射线系统
PMA编号：P130025 · 2023-10-12
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器械摘要
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.
常见问题
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.
相关临床试验
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官方来源
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