Ablation-fit
K号: K222938 · 2023-09-12
广告
器械摘要
Ablation-fit is the device name listed in this FDA 510(k) record. The listed applicant is R.A.W. S.R.L. It received FDA 510(k) clearance on 2023-09-12 under 510(k) number K222938. The device is classified under product code QTZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Ablation-fit?
Ablation-fit is a medical device that received FDA 510(k) clearance on 2023-09-12. The listed applicant is R.A.W. S.R.L. The 510(k) number is K222938.
When did Ablation-fit receive FDA 510(k) clearance?
Ablation-fit received FDA 510(k) clearance on 2023-09-12, under 510(k) number K222938.
Who is the listed applicant for Ablation-fit?
The FDA 510(k) record lists R.A.W. S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ablation-fit?
The FDA product code for Ablation-fit is QTZ.
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：QTZ）
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。
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。
广告