再生处理DePuy Mitek消融棒
K号: K173740 · 2018-03-19
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器械摘要
Reprocessed DePuy Mitek Ablation Wand is the device name listed in this FDA 510(k) record. The listed applicant is Renovo, Inc.. It received FDA 510(k) clearance on 2018-03-19 under 510(k) number K173740. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Reprocessed DePuy Mitek Ablation Wand?
Reprocessed DePuy Mitek Ablation Wand is a medical device that received FDA 510(k) clearance on 2018-03-19. The listed applicant is Renovo, Inc.. The 510(k) number is K173740.
When did Reprocessed DePuy Mitek Ablation Wand receive FDA 510(k) clearance?
Reprocessed DePuy Mitek Ablation Wand received FDA 510(k) clearance on 2018-03-19, under 510(k) number K173740.
Who is the listed applicant for Reprocessed DePuy Mitek Ablation Wand?
The FDA 510(k) record lists Renovo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reprocessed DePuy Mitek Ablation Wand?
The FDA product code for Reprocessed DePuy Mitek Ablation Wand is NUJ.
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Renovo, 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：NUJ）
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。
K232511Medline ReNewal Reprocessed LigaSure 精确分离器，纳米涂层（LF2019）Surgical Instrument Service and Savings, Inc.K230251再处理的LigaSure弯曲，小口，开放式密封/分离器（LF1212A）Stryker Sustainability SolutionsK220411再处理的LigaSure弯曲，小口，开放式密封/分离器（LF1212A）Stryker Sustainability SolutionsK211203Green OR Reprocessed Aquamantys Bipolar SealerGreen Or, LLCK191073Vein360 静脉射频消融（RFA）导管Vein 360, LLCK182588Medline ReNewal Reprocessed LigaSure 马里兰州颚式密封/分隔器Surgical Instrument Service and Savings Inc.(Dba Medline Ren
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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