Stimucel 系统,Stimucel 发电机,Stimucel 治疗棒,Stimucel 治疗器
K号: K162721 · 2016-12-22
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器械摘要
常见问题
What is the Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator?
Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator is a medical device that received FDA 510(k) clearance on 2016-12-22. The listed applicant is Alliqua Biomedical, Inc.. The 510(k) number is K162721.
When did Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator receive FDA 510(k) clearance?
Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator received FDA 510(k) clearance on 2016-12-22, under 510(k) number K162721.
Who is the listed applicant for Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator?
The FDA 510(k) record lists Alliqua Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator?
The FDA product code for Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator is NRB.
相关临床试验
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列明Alliqua Biomedical, 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。
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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