FDA 510(k)POCKET TENS (EP-300)
K号: K242815 · 2024-12-17
决定日期2024-12-17
产品代码NUH
咨询委员会NE
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决定实质等同
器械摘要
POCKET TENS (EP-300) is the device name listed in this FDA 510(k) record. The listed applicant is Hivox Biotek, Inc.. It received FDA 510(k) clearance on 2024-12-17 under 510(k) number K242815. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the POCKET TENS (EP-300)?
POCKET TENS (EP-300) is a medical device that received FDA 510(k) clearance on 2024-12-17. The listed applicant is Hivox Biotek, Inc.. The 510(k) number is K242815.
When did POCKET TENS (EP-300) receive FDA 510(k) clearance?
POCKET TENS (EP-300) received FDA 510(k) clearance on 2024-12-17, under 510(k) number K242815.
Who is the listed applicant for POCKET TENS (EP-300)?
The FDA 510(k) record lists Hivox Biotek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POCKET TENS (EP-300)?
The FDA product code for POCKET TENS (EP-300) is NUH.
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列明Hivox Biotek, Inc.为申报人的其他记录
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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。
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