Cadwell Guardian
K号: K230415 · 2023-08-17
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决定日期2023-08-17
产品代码GWF
咨询委员会NE
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器械摘要
Cadwell Guardian is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Industries, Inc.. It received FDA 510(k) clearance on 2023-08-17 under 510(k) number K230415. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Cadwell Guardian?
Cadwell Guardian is a medical device that received FDA 510(k) clearance on 2023-08-17. The listed applicant is Cadwell Industries, Inc.. The 510(k) number is K230415.
When did Cadwell Guardian receive FDA 510(k) clearance?
Cadwell Guardian received FDA 510(k) clearance on 2023-08-17, under 510(k) number K230415.
Who is the listed applicant for Cadwell Guardian?
The FDA 510(k) record lists Cadwell Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cadwell Guardian?
The FDA product code for Cadwell Guardian is GWF.
相关临床试验
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列明Cadwell Industries, Inc.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：GWF）
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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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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