XOD 气热射频设备
K号: K242175 · 2025-02-27
广告
器械摘要
XOD Diathermia Radiofrequency Device is the device name listed in this FDA 510(k) record. The listed applicant is Xod, Inc.. It received FDA 510(k) clearance on 2025-02-27 under 510(k) number K242175. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the XOD Diathermia Radiofrequency Device?
XOD Diathermia Radiofrequency Device is a medical device that received FDA 510(k) clearance on 2025-02-27. The listed applicant is Xod, Inc.. The 510(k) number is K242175.
When did XOD Diathermia Radiofrequency Device receive FDA 510(k) clearance?
XOD Diathermia Radiofrequency Device received FDA 510(k) clearance on 2025-02-27, under 510(k) number K242175.
Who is the listed applicant for XOD Diathermia Radiofrequency Device?
The FDA 510(k) record lists Xod, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XOD Diathermia Radiofrequency Device?
The FDA product code for XOD Diathermia Radiofrequency Device is PBX.
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：PBX）
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