DP4微针治疗仪
K号: K221070 · 2022-12-20
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器械摘要
DP4 Microneedling device is the device name listed in this FDA 510(k) record. The listed applicant is Equipmed USA, LLC. It received FDA 510(k) clearance on 2022-12-20 under 510(k) number K221070. The device is classified under product code QAI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DP4 Microneedling device?
DP4 Microneedling device is a medical device that received FDA 510(k) clearance on 2022-12-20. The listed applicant is Equipmed USA, LLC. The 510(k) number is K221070.
When did DP4 Microneedling device receive FDA 510(k) clearance?
DP4 Microneedling device received FDA 510(k) clearance on 2022-12-20, under 510(k) number K221070.
Who is the listed applicant for DP4 Microneedling device?
The FDA 510(k) record lists Equipmed USA, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DP4 Microneedling device?
The FDA product code for DP4 Microneedling device is QAI.
相关临床试验
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：QAI）
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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