淋巴结定位系统，在哨兵活检程序期间
PMA编号：P160053 · 2026-05-18
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决定日期2026-05-18
PMA 编号P160053
产品代码PUV
设备分类第3类
医疗专科U
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
器械摘要
Lymph node location system during sentinel biopsy procedure is the device name listed in this FDA 510(k) record. The listed applicant is Endomagnetics Ltd.,. It received FDA 510(k) clearance on 2026-05-18. The device is classified under product code PUV. It was reviewed by the SU advisory panel.
常见问题
What is the Lymph node location system during sentinel biopsy procedure?
Lymph node location system during sentinel biopsy procedure is a medical device that received FDA 510(k) clearance on 2026-05-18. The listed applicant is Endomagnetics Ltd.,.
When did Lymph node location system during sentinel biopsy procedure receive FDA 510(k) clearance?
The clearance date for Lymph node location system during sentinel biopsy procedure can be found in the official FDA records.
Who is the listed applicant for Lymph node location system during sentinel biopsy procedure?
The FDA 510(k) record lists Endomagnetics Ltd., as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lymph node location system during sentinel biopsy procedure?
The FDA product code for Lymph node location system during sentinel biopsy procedure is PUV.
相关临床试验
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官方来源
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