SIDEKICK and USHER Support Catheters
K号: K161986 · 2016-08-04
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器械摘要
SIDEKICK and USHER Support Catheters is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2016-08-04 under 510(k) number K161986. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SIDEKICK and USHER Support Catheters?
SIDEKICK and USHER Support Catheters is a medical device that received FDA 510(k) clearance on 2016-08-04. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K161986.
When did SIDEKICK and USHER Support Catheters receive FDA 510(k) clearance?
SIDEKICK and USHER Support Catheters received FDA 510(k) clearance on 2016-08-04, under 510(k) number K161986.
Who is the listed applicant for SIDEKICK and USHER Support Catheters?
The FDA 510(k) record lists Bard Peripheral Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIDEKICK and USHER Support Catheters?
The FDA product code for SIDEKICK and USHER Support Catheters is DQY.
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列明Bard Peripheral Vascular, Inc.为申报人的其他记录
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相关器械（代码：DQY）
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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