维图瑞安终极吸痰器
K号: K161722 · 2016-07-26
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决定日期2016-07-26
产品代码QPB
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
VITRUVIAN ULTIMATE ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Black & Black Surgical, Inc.. It received FDA 510(k) clearance on 2016-07-26 under 510(k) number K161722. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VITRUVIAN ULTIMATE ASPIRATOR?
VITRUVIAN ULTIMATE ASPIRATOR is a medical device that received FDA 510(k) clearance on 2016-07-26. The listed applicant is Black & Black Surgical, Inc.. The 510(k) number is K161722.
When did VITRUVIAN ULTIMATE ASPIRATOR receive FDA 510(k) clearance?
VITRUVIAN ULTIMATE ASPIRATOR received FDA 510(k) clearance on 2016-07-26, under 510(k) number K161722.
Who is the listed applicant for VITRUVIAN ULTIMATE ASPIRATOR?
The FDA 510(k) record lists Black & Black Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITRUVIAN ULTIMATE ASPIRATOR?
The FDA product code for VITRUVIAN ULTIMATE ASPIRATOR is QPB.
相关临床试验
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。
列明Black & Black Surgical, 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。
相关器械（代码：QPB）
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。
K254135脂塑术艺术家NOUVAG AGK261710AYON™ Power Liposuction Cannulas和AYON™ Power Liposuction Cannula AdaptorsApyx Medical CorporationK251944Lipocosm谐波系统Lipocosm, LLCK253396AYON 身体塑形系统® (AYON SYSTEM)Apyx Medical CorporationK252495LSSA (NP-200)Newpong Co., Ltd.K244050AYON 身体塑形系统 (AYON SYSTEM)Apyx Medical Corporation
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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