INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set
K号: K153272 · 2016-07-09
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器械摘要
常见问题
What is the INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set?
INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set is a medical device that received FDA 510(k) clearance on 2016-07-09. The listed applicant is Relievant Medsystems. The 510(k) number is K153272.
When did INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set receive FDA 510(k) clearance?
INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set received FDA 510(k) clearance on 2016-07-09, under 510(k) number K153272.
Who is the listed applicant for INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set?
The FDA 510(k) record lists Relievant Medsystems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set?
The FDA product code for INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set is GXI.
相关临床试验
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列明Relievant Medsystems为申报人的其他记录
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。
相关器械(代码:GXI)
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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