STIMPOD NMS460 神经刺激器
K号: K252712 · 2026-05-28
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决定日期2026-05-28
产品代码GZJ
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
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器械摘要
STIMPOD NMS460 Nerve Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Algiamed Technologies USA, Inc.. It received FDA 510(k) clearance on 2026-05-28 under 510(k) number K252712. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the STIMPOD NMS460 Nerve Stimulator?
STIMPOD NMS460 Nerve Stimulator is a medical device that received FDA 510(k) clearance on 2026-05-28. The listed applicant is Algiamed Technologies USA, Inc.. The 510(k) number is K252712.
When did STIMPOD NMS460 Nerve Stimulator receive FDA 510(k) clearance?
STIMPOD NMS460 Nerve Stimulator received FDA 510(k) clearance on 2026-05-28, under 510(k) number K252712.
Who is the listed applicant for STIMPOD NMS460 Nerve Stimulator?
The FDA 510(k) record lists Algiamed Technologies USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STIMPOD NMS460 Nerve Stimulator?
The FDA product code for STIMPOD NMS460 Nerve Stimulator is GZJ.
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相关器械（代码：GZJ）
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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