T65 (9016E061-)
K号: K252032 · 2025-07-30
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决定日期2025-07-30
产品代码OBP
咨询委员会NE
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决定实质等同
器械摘要
T65 (9016E061-) is the device name listed in this FDA 510(k) record. The listed applicant is Tonica Elektronik A/S. It received FDA 510(k) clearance on 2025-07-30 under 510(k) number K252032. 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 T65 (9016E061-)?
T65 (9016E061-) is a medical device that received FDA 510(k) clearance on 2025-07-30. The listed applicant is Tonica Elektronik A/S. The 510(k) number is K252032.
When did T65 (9016E061-) receive FDA 510(k) clearance?
T65 (9016E061-) received FDA 510(k) clearance on 2025-07-30, under 510(k) number K252032.
Who is the listed applicant for T65 (9016E061-)?
The FDA 510(k) record lists Tonica Elektronik A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T65 (9016E061-)?
The FDA product code for T65 (9016E061-) is OBP.
列明Tonica Elektronik A/S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: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。
K260396KCS rTMS治疗系统(经颅磁刺激器)(MetaStim 100,MetaStim 100A)Fidelity BioPharma Co.K260691BTL-699BTL Industries, Inc.K261228QuickVision Ultimate 经颅磁刺激器Brain Ultimate, Inc.K260189MagVenture加速TMS(aTMS)治疗系统Tonica Elektronik A/SK260560Apollo TMS 疗法系统;Apollo light TMS 疗法系统Mag & More GmbHK253098Nexstim 导航脑刺激 (NBS) 6 系统 (NBS6)Nexstim Oyj
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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