CrossCath Support Catheter
K号: K161801 · 2016-07-29
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器械摘要
CrossCath Support Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2016-07-29 under 510(k) number K161801. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CrossCath Support Catheter?
CrossCath Support Catheter is a medical device that received FDA 510(k) clearance on 2016-07-29. The listed applicant is Cook Incorporated. The 510(k) number is K161801.
When did CrossCath Support Catheter receive FDA 510(k) clearance?
CrossCath Support Catheter received FDA 510(k) clearance on 2016-07-29, under 510(k) number K161801.
Who is the listed applicant for CrossCath Support Catheter?
The FDA 510(k) record lists Cook Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CrossCath Support Catheter?
The FDA product code for CrossCath Support Catheter is KRA.
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列明Cook Incorporated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：KRA）
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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