Renasys Edge
K号: K231939 · 2024-05-24
广告
决定日期2024-05-24
产品代码OMP
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
Renasys Edge is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Medical, Ltd.. It received FDA 510(k) clearance on 2024-05-24 under 510(k) number K231939. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Renasys Edge?
Renasys Edge is a medical device that received FDA 510(k) clearance on 2024-05-24. The listed applicant is Smith & Nephew Medical, Ltd.. The 510(k) number is K231939.
When did Renasys Edge receive FDA 510(k) clearance?
Renasys Edge received FDA 510(k) clearance on 2024-05-24, under 510(k) number K231939.
Who is the listed applicant for Renasys Edge?
FDA 510(k)记录将史密斯·奈普医疗有限公司列为申请人。这本身并不能确立该设备的制造商。
What is the FDA product code for Renasys Edge?
The FDA product code for Renasys Edge is OMP.
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Smith & Nephew Medical, Ltd.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：OMP）
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。
K261338RENASYS DYNAFLOW 套件（66807741）Smith & Nephew Medical, Ltd.K253263ConvaVAC™ 负压伤口治疗系统Convatec Limited, Gdc BuildingK253199CURASYS 2 (EMDN0003)CG Bio Co., Ltd.K260646RENASYS EDGE (66803126)Smith & Nephew Medical, Ltd.K261291Nisus NPWT 罐 500-毫升 (CPC-500)Cork MedicalK254019伤口基因NPWT系统Bechtel Medical, Inc.
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