XCELLARISPRO TWIST 微针滚轮设备
K号: K241790 · 2025-03-06
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器械摘要
XCELLARISPRO TWIST microneedling device is the device name listed in this FDA 510(k) record. The listed applicant is Dermaroller GmbH. It received FDA 510(k) clearance on 2025-03-06 under 510(k) number K241790. 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 XCELLARISPRO TWIST microneedling device?
XCELLARISPRO TWIST microneedling device is a medical device that received FDA 510(k) clearance on 2025-03-06. The listed applicant is Dermaroller GmbH. The 510(k) number is K241790.
When did XCELLARISPRO TWIST microneedling device receive FDA 510(k) clearance?
XCELLARISPRO TWIST microneedling device received FDA 510(k) clearance on 2025-03-06, under 510(k) number K241790.
Who is the listed applicant for XCELLARISPRO TWIST microneedling device?
The FDA 510(k) record lists Dermaroller GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XCELLARISPRO TWIST microneedling device?
The FDA product code for XCELLARISPRO TWIST 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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