FDA 510(k)

AnyScan 3.0 NM 扫描仪系列

K号: K253844 · 2025-12-30

决定日期2025-12-30

产品代码KPS

咨询委员会RA

决定实质等同

器械摘要

AnyScan 3.0 NM Scanner Family is the device name listed in this FDA 510(k) record. The listed applicant is Mediso Medical Imaging Systems, Ltd.. It received FDA 510(k) clearance on 2025-12-30 under 510(k) number K253844. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AnyScan 3.0 NM Scanner Family?

AnyScan 3.0 NM Scanner Family is a medical device that received FDA 510(k) clearance on 2025-12-30. The listed applicant is Mediso Medical Imaging Systems, Ltd.. The 510(k) number is K253844.

When did AnyScan 3.0 NM Scanner Family receive FDA 510(k) clearance?

AnyScan 3.0 NM Scanner Family received FDA 510(k) clearance on 2025-12-30, under 510(k) number K253844.

Who is the listed applicant for AnyScan 3.0 NM Scanner Family?

The FDA 510(k) record lists Mediso Medical Imaging Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AnyScan 3.0 NM Scanner Family?

The FDA product code for AnyScan 3.0 NM Scanner Family is KPS.

相关器械（代码：KPS）

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器械摘要

常见问题

相关临床试验

相关器械（代码：KPS）

官方来源