RENASYS-G Gauze Dressing Kits with Soft Port
K号: K162129 · 2016-08-31
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器械摘要
RENASYS-G Gauze Dressing Kits with Soft Port is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2016-08-31 under 510(k) number K162129. 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-G Gauze Dressing Kits with Soft Port?
RENASYS-G Gauze Dressing Kits with Soft Port is a medical device that received FDA 510(k) clearance on 2016-08-31. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K162129.
When did RENASYS-G Gauze Dressing Kits with Soft Port receive FDA 510(k) clearance?
RENASYS-G Gauze Dressing Kits with Soft Port received FDA 510(k) clearance on 2016-08-31, under 510(k) number K162129.
Who is the listed applicant for RENASYS-G Gauze Dressing Kits with Soft Port?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RENASYS-G Gauze Dressing Kits with Soft Port?
The FDA product code for RENASYS-G Gauze Dressing Kits with Soft Port is OMP.
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列明Smith & Nephew, 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。
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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。
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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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