Axon 疗法
K号: K233364 · 2024-01-10
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决定日期2024-01-10
产品代码QPL
咨询委员会NE
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器械摘要
Axon Therapy is the device name listed in this FDA 510(k) record. The listed applicant is Neuralace Medical, Inc.. It received FDA 510(k) clearance on 2024-01-10 under 510(k) number K233364. The device is classified under product code QPL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Axon Therapy?
Axon Therapy is a medical device that received FDA 510(k) clearance on 2024-01-10. The listed applicant is Neuralace Medical, Inc.. The 510(k) number is K233364.
When did Axon Therapy receive FDA 510(k) clearance?
Axon Therapy received FDA 510(k) clearance on 2024-01-10, under 510(k) number K233364.
Who is the listed applicant for Axon Therapy?
The FDA 510(k) record lists Neuralace Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Axon Therapy?
The FDA product code for Axon Therapy is QPL.
相关临床试验
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列明Neuralace Medical, 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。
相关器械（代码：QPL）
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。
K250309BTL-199BTL Industries, Inc.K250286Rapid2 磁刺激器（Magstim Rapid2，Magstim Super Rapid2，Magstim Super Rapid2 Plus1）The Magstim Company LimitedK241785StarFormer (M008-3T)Fotona D.O.O.K230014MagVenture疼痛治疗：MagPro R30，MagPro R30带MagOption，MagPro X100，MagPro X100带MagOptionTonica Elektronik A/SK210021Axon 疗法Neuralace Medical, Inc.
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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