联合高频X射线源
K号: K222258 · 2022-11-01
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器械摘要
Combined High Frequency X-ray Source is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Powersite Electric Co., Ltd.. It received FDA 510(k) clearance on 2022-11-01 under 510(k) number K222258. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Combined High Frequency X-ray Source?
Combined High Frequency X-ray Source is a medical device that received FDA 510(k) clearance on 2022-11-01. The listed applicant is Suzhou Powersite Electric Co., Ltd.. The 510(k) number is K222258.
When did Combined High Frequency X-ray Source receive FDA 510(k) clearance?
Combined High Frequency X-ray Source received FDA 510(k) clearance on 2022-11-01, under 510(k) number K222258.
Who is the listed applicant for Combined High Frequency X-ray Source?
The FDA 510(k) record lists Suzhou Powersite Electric Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Combined High Frequency X-ray Source?
The FDA product code for Combined High Frequency X-ray Source is IZL.
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：IZL）
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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