THUNDERBEAT Open Fine Jaw
K号: K151743 · 2016-02-26
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决定日期2016-02-26
产品代码GEI
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
THUNDERBEAT Open Fine Jaw is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2016-02-26 under 510(k) number K151743. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the THUNDERBEAT Open Fine Jaw?
THUNDERBEAT Open Fine Jaw is a medical device that received FDA 510(k) clearance on 2016-02-26. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K151743.
When did THUNDERBEAT Open Fine Jaw receive FDA 510(k) clearance?
THUNDERBEAT Open Fine Jaw received FDA 510(k) clearance on 2016-02-26, under 510(k) number K151743.
Who is the listed applicant for THUNDERBEAT Open Fine Jaw?
FDA 510(k)记录中列出Olympus Medical Systems Corp.为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for THUNDERBEAT Open Fine Jaw?
The FDA product code for THUNDERBEAT Open Fine Jaw is GEI.
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列明Olympus Medical Systems Corp.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。
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相关器械（代码：GEI）
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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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