假肢，睾丸
PMA编号：P020003 · 2026-07-21
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决定日期2026-07-21
PMA 编号P020003
产品代码FAF
设备分类第3类
医疗专科G
法规编号21 CFR 8
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
器械摘要
Prosthesis, testicular is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast Corp.. It received FDA 510(k) clearance on 2026-07-21. The device is classified under product code FAF. It was reviewed by the GU advisory panel.
常见问题
What is the Prosthesis, testicular?
Prosthesis, testicular is a medical device that received FDA 510(k) clearance on 2026-07-21. The listed applicant is Coloplast Corp..
When did Prosthesis, testicular receive FDA 510(k) clearance?
The clearance date for Prosthesis, testicular can be found in the official FDA records.
谁是被列出的睾丸假体申请者？
The FDA 510(k) record lists Coloplast Corp. as the applicant. This does not by itself establish the device manufacturer.
什么是假体、睾丸的FDA产品代码？
FDA产品代码，假体，睾丸为FAF。
相关临床试验
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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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