原位荧光杂交，染色体 17p 缺失（TP53）
PMA编号：P150041 · 2026-02-18
广告
决定日期2026-02-18
PMA 编号P150041
产品代码PNK
设备分类第3类
医疗专科U
咨询委员会PA
请注意，由于您没有提供具体的医疗设备监管文本，我无法提供准确的翻译。如果您能提供具体的文本内容，我将能够为您提供准确的翻译。
器械摘要
Fluorescence in situ hybridization, chromosome 17p deletion (TP53) is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Molecular, Inc.. It received FDA 510(k) clearance on 2026-02-18. The device is classified under product code PNK. It was reviewed by the PA advisory panel.
常见问题
What is the Fluorescence in situ hybridization, chromosome 17p deletion (TP53)?
Fluorescence in situ hybridization, chromosome 17p deletion (TP53) is a medical device that received FDA 510(k) clearance on 2026-02-18. The listed applicant is Abbott Molecular, Inc..
When did Fluorescence in situ hybridization, chromosome 17p deletion (TP53) receive FDA 510(k) clearance?
The clearance date for Fluorescence in situ hybridization, chromosome 17p deletion (TP53) can be found in the official FDA records.
Who is the listed applicant for Fluorescence in situ hybridization, chromosome 17p deletion (TP53)?
The FDA 510(k) record lists Abbott Molecular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fluorescence in situ hybridization, chromosome 17p deletion (TP53)?
The FDA product code for Fluorescence in situ hybridization, chromosome 17p deletion (TP53) is PNK.
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。
广告