威金斯医疗外科器械
K号: K200383 · 2020-07-21
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决定日期2020-07-21
产品代码HAE
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
Wiggins Medical Surgical Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Wiggins Medical. It received FDA 510(k) clearance on 2020-07-21 under 510(k) number K200383. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Wiggins Medical Surgical Instruments?
Wiggins Medical Surgical Instruments is a medical device that received FDA 510(k) clearance on 2020-07-21. The listed applicant is Wiggins Medical. The 510(k) number is K200383.
When did Wiggins Medical Surgical Instruments receive FDA 510(k) clearance?
Wiggins Medical Surgical Instruments received FDA 510(k) clearance on 2020-07-21, under 510(k) number K200383.
Who is the listed applicant for Wiggins Medical Surgical Instruments?
The FDA 510(k) record lists Wiggins Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Wiggins Medical Surgical Instruments?
The FDA product code for Wiggins Medical Surgical Instruments is HAE.
相关临床试验
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相关器械（代码：HAE）
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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