A1417MCW/A1717MCW/F1417MCW
K号: K223930 · 2023-03-06
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器械摘要
A1417MCW/A1717MCW/F1417MCW is the device name listed in this FDA 510(k) record. The listed applicant is H&abyz Co., Ltd.. It received FDA 510(k) clearance on 2023-03-06 under 510(k) number K223930. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the A1417MCW/A1717MCW/F1417MCW?
A1417MCW/A1717MCW/F1417MCW is a medical device that received FDA 510(k) clearance on 2023-03-06. The listed applicant is H&abyz Co., Ltd.. The 510(k) number is K223930.
When did A1417MCW/A1717MCW/F1417MCW receive FDA 510(k) clearance?
A1417MCW/A1717MCW/F1417MCW received FDA 510(k) clearance on 2023-03-06, under 510(k) number K223930.
Who is the listed applicant for A1417MCW/A1717MCW/F1417MCW?
The FDA 510(k) record lists H&abyz Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A1417MCW/A1717MCW/F1417MCW?
The FDA product code for A1417MCW/A1717MCW/F1417MCW is MQB.
列明H&abyz 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：MQB）
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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