AccuCath Intravascular Catheter
K号: K162894 · 2016-11-15
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器械摘要
AccuCath Intravascular Catheter 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 2016-11-15 under 510(k) number K162894. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AccuCath Intravascular Catheter?
AccuCath Intravascular Catheter is a medical device that received FDA 510(k) clearance on 2016-11-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162894.
When did AccuCath Intravascular Catheter receive FDA 510(k) clearance?
AccuCath Intravascular Catheter received FDA 510(k) clearance on 2016-11-15, under 510(k) number K162894.
Who is the listed applicant for AccuCath Intravascular Catheter?
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 AccuCath Intravascular Catheter?
The FDA product code for AccuCath Intravascular Catheter is FOZ.
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列明C.R. Bard, Inc.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。
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相关器械（代码：FOZ）
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
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