FDA 510(k)

Elecsys CYFRA 21-1，Elecsys CYFRA 21-1 CalSet，PreciControl 肿瘤标志物

K号: K160915 · 2016-12-14

决定日期2016-12-14

产品代码OVK

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决定实质等同

器械摘要

Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics. It received FDA 510(k) clearance on 2016-12-14 under 510(k) number K160915. The device is classified under product code OVK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker?

Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker is a medical device that received FDA 510(k) clearance on 2016-12-14. The listed applicant is Roche Diagnostics. The 510(k) number is K160915.

When did Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker receive FDA 510(k) clearance?

Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker received FDA 510(k) clearance on 2016-12-14, under 510(k) number K160915.

Who is the listed applicant for Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker?

FDA 510(k)记录显示罗氏诊断公司为申请人。这本身并不能确立该设备的制造商。

What is the FDA product code for Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker?

The FDA product code for Elecsys CYFRA 21-1, Elecsys CYFRA 21-1 CalSet, PreciControl Tumor Marker is OVK.

列明Roche Diagnostics为申报人的其他记录

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