M-Y Sheath
K号: K190369 · 2019-04-17
广告
决定日期2019-04-17
产品代码DYB
咨询委员会CV
请注意,由于原文未提供具体内容,以下是一个示例翻译:
---
产品名称:[产品名称]
公司名称:[公司名称]
FDA批准号:[FDA批准号]
510(k)申请号:[510(k)申请号]
PMA申请号:[PMA申请号]
临床试验注册号:[NCT]
PubMed ID:[PMID]
产品标识符:[标识符]
产品URL:[URL]
---
请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
决定实质等同
器械摘要
M-Y Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Ram Medical Innovations, Inc.. It received FDA 510(k) clearance on 2019-04-17 under 510(k) number K190369. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the M-Y Sheath?
M-Y Sheath is a medical device that received FDA 510(k) clearance on 2019-04-17. The listed applicant is Ram Medical Innovations, Inc.. The 510(k) number is K190369.
When did M-Y Sheath receive FDA 510(k) clearance?
M-Y Sheath received FDA 510(k) clearance on 2019-04-17, under 510(k) number K190369.
Who is the listed applicant for M-Y Sheath?
The FDA 510(k) record lists Ram Medical Innovations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for M-Y Sheath?
The FDA product code for M-Y Sheath is DYB.
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。
相关器械(代码:DYB)
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。
K253526NAMIC 扩张器和套管Medline Industries, LPK261529微穿刺套件/微穿刺接入套件/微穿刺引导器套装/微引导器套件/微引导器套件(SIS05C);微穿刺套件/微穿刺接入套件/微穿刺引导器套装/微引导器套件/微引导器套件(IS01);引导器套件/微引导器套件/引导器套装/微引导器套装/微引导器鞘套装/引导器鞘套装(NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line 可撕开引导器Health Line International CorporationK261492FieldFlex 可弯曲鞘CenterPoint Systems, LLCK260606Echo 大口径引导鞘Echo Medical, LLC
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。
广告