自动乳腺超声
PMA编号：P110006 · 2025-02-04
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器械摘要
Automated breast ultrasound is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2025-02-04. The device is classified under product code PAA. It was reviewed by the RA advisory panel.
常见问题
What is the Automated breast ultrasound?
Automated breast ultrasound is a medical device that received FDA 510(k) clearance on 2025-02-04. The listed applicant is GE Healthcare.
When did Automated breast ultrasound receive FDA 510(k) clearance?
The clearance date for Automated breast ultrasound can be found in the official FDA records.
Who is the listed applicant for Automated breast ultrasound?
The FDA 510(k) record lists GE Healthcare as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Automated breast ultrasound?
The FDA product code for Automated breast ultrasound is PAA.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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