AXUS ES-5 电针治疗仪
K号: K200636 · 2021-02-03
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器械摘要
AXUS ES-5 Electro-Acupuncture Device is the device name listed in this FDA 510(k) record. The listed applicant is Lhasa Oms, Inc.. It received FDA 510(k) clearance on 2021-02-03 under 510(k) number K200636. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.
常见问题
What is the AXUS ES-5 Electro-Acupuncture Device?
AXUS ES-5 Electro-Acupuncture Device is a medical device that received FDA 510(k) clearance on 2021-02-03. The listed applicant is Lhasa Oms, Inc.. The 510(k) number is K200636.
When did AXUS ES-5 Electro-Acupuncture Device receive FDA 510(k) clearance?
AXUS ES-5 Electro-Acupuncture Device received FDA 510(k) clearance on 2021-02-03, under 510(k) number K200636.
Who is the listed applicant for AXUS ES-5 Electro-Acupuncture Device?
The FDA 510(k) record lists Lhasa Oms, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXUS ES-5 Electro-Acupuncture Device?
The FDA product code for AXUS ES-5 Electro-Acupuncture Device is BWK.
相关临床试验
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相关器械（代码：BWK）
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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