NQ TMS for MDD (NQv1-MU-01)
K号: K232688 · 2023-12-29
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决定日期2023-12-29
产品代码OBP
咨询委员会NE
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器械摘要
NQ TMS for MDD (NQv1-MU-01) is the device name listed in this FDA 510(k) record. The listed applicant is Neuroqore, Inc.. It received FDA 510(k) clearance on 2023-12-29 under 510(k) number K232688. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the NQ TMS for MDD (NQv1-MU-01)?
NQ TMS for MDD (NQv1-MU-01) is a medical device that received FDA 510(k) clearance on 2023-12-29. The listed applicant is Neuroqore, Inc.. The 510(k) number is K232688.
When did NQ TMS for MDD (NQv1-MU-01) receive FDA 510(k) clearance?
NQ TMS for MDD (NQv1-MU-01) received FDA 510(k) clearance on 2023-12-29, under 510(k) number K232688.
Who is the listed applicant for NQ TMS for MDD (NQv1-MU-01)?
The FDA 510(k) record lists Neuroqore, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NQ TMS for MDD (NQv1-MU-01)?
The FDA product code for NQ TMS for MDD (NQv1-MU-01) is OBP.
相关器械（代码：OBP）
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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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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