Well-Life迷你经皮神经电刺激器(WL-23XXC/WL-23XXE系列)
K号: K220524 · 2022-08-04
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器械摘要
常见问题
What is the Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)?
Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series) is a medical device that received FDA 510(k) clearance on 2022-08-04. The listed applicant is Well-Life Healthcare Limited. The 510(k) number is K220524.
When did Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series) receive FDA 510(k) clearance?
Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series) received FDA 510(k) clearance on 2022-08-04, under 510(k) number K220524.
Who is the listed applicant for Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)?
The FDA 510(k) record lists Well-Life Healthcare Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)?
The FDA product code for Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series) is NUH.
相关临床试验
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列明Well-Life Healthcare Limited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:NUH)
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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