FDA 510(k)

TruSPECT 放射影像处理站

K号: K212230 · 2021-08-16

决定日期2021-08-16

产品代码LLZ

咨询委员会RA

决定实质等同

器械摘要

TruSPECT Radiological Image Processing Station is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum Dynamics Medical, Ltd.. It received FDA 510(k) clearance on 2021-08-16 under 510(k) number K212230. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TruSPECT Radiological Image Processing Station?

TruSPECT Radiological Image Processing Station is a medical device that received FDA 510(k) clearance on 2021-08-16. The listed applicant is Spectrum Dynamics Medical, Ltd.. The 510(k) number is K212230.

When did TruSPECT Radiological Image Processing Station receive FDA 510(k) clearance?

TruSPECT Radiological Image Processing Station received FDA 510(k) clearance on 2021-08-16, under 510(k) number K212230.

Who is the listed applicant for TruSPECT Radiological Image Processing Station?

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

What is the FDA product code for TruSPECT Radiological Image Processing Station?

The FDA product code for TruSPECT Radiological Image Processing Station is LLZ.

列明Spectrum Dynamics Medical, Ltd.为申报人的其他记录

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。

K254001VERITON CT 300系列数字SPECT/CT系统（VERITON CT 316/364）；VERITON CT 400系列数字SPECT/CT系统（VERITON CT 416/464）K253532TruSPECT处理站 K230600VERITON CT 300系列数字SPECT/CT系统（VERITON CT 316/364）；VERITON CT 400系列数字SPECT/CT系统（VERITON CT 416/464）K190457威瑞通全身SPECT/CT系统 K182484威瑞通全身SPECT/CT系统 K180514维瑞顿NM

查看所有 8 个设备 →

官方来源

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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。