KIT, 人类乳头瘤病毒检测
PMA编号：P230003 · 2026-09-02
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决定日期2026-09-02
PMA 编号P230003
产品代码MAQ
设备分类第3类
医疗专科U
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器械摘要
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS 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 2026-09-02. The device is classified under product code MAQ. It was reviewed by the MI advisory panel.
常见问题
What is the KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS?
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS is a medical device that received FDA 510(k) clearance on 2026-09-02. The listed applicant is Abbott Molecular, Inc..
When did KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS receive FDA 510(k) clearance?
The clearance date for KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS can be found in the official FDA records.
KIT，DNA检测，人乳头瘤病毒检测的申请人是谁？
The FDA 510(k) record lists Abbott Molecular, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA产品代码是多少，针对KIT、DNA检测、人乳头瘤病毒？
FDA产品代码为KIT、DNA检测、人乳头瘤病毒的产品是MAQ。
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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