Pinpoint GT Introducer Needle
K号: K162769 · 2016-11-04
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器械摘要
Pinpoint GT Introducer Needle is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2016-11-04 under 510(k) number K162769. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Pinpoint GT Introducer Needle?
Pinpoint GT Introducer Needle is a medical device that received FDA 510(k) clearance on 2016-11-04. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162769.
When did Pinpoint GT Introducer Needle receive FDA 510(k) clearance?
Pinpoint GT Introducer Needle received FDA 510(k) clearance on 2016-11-04, under 510(k) number K162769.
Who is the listed applicant for Pinpoint GT Introducer Needle?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pinpoint GT Introducer Needle?
The FDA product code for Pinpoint GT Introducer Needle is DYB.
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列明C.R. Bard, Inc.为申报人的其他记录
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相关器械（代码：DYB）
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。
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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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