经皮神经电刺激与电肌肉刺激(经皮神经电刺激和肌肉刺激器)(JT8012, JT8012B)
K号: K250053 · 2025-05-09
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器械摘要
常见问题
What is the TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)?
TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) is a medical device that received FDA 510(k) clearance on 2025-05-09. The listed applicant is Shenzhen Jiantuo Electronics Co., Ltd.. The 510(k) number is K250053.
When did TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) receive FDA 510(k) clearance?
TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) received FDA 510(k) clearance on 2025-05-09, under 510(k) number K250053.
Who is the listed applicant for TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)?
The FDA 510(k) record lists Shenzhen Jiantuo Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)?
The FDA product code for TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) is NUH.
相关临床试验
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。
列明Shenzhen Jiantuo Electronics Co., Ltd.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: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。
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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