ADD
K号: K203188 · 2021-03-12
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器械摘要
ADD 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 2021-03-12 under 510(k) number K203188. 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 ADD?
ADD is a medical device that received FDA 510(k) clearance on 2021-03-12. The listed applicant is H&abyz Co., Ltd.. The 510(k) number is K203188.
When did ADD receive FDA 510(k) clearance?
ADD received FDA 510(k) clearance on 2021-03-12, under 510(k) number K203188.
Who is the listed applicant for ADD?
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 ADD?
The FDA product code for ADD is MQB.
相关 PubMed 文献
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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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