膀胱EpiCheck DNA提取试剂盒,NX899090-01C,膀胱EpiCheck测试试剂盒,NX899090-02C,膀胱EpiCheck软件,NX899090-03C
K号: K203245 · 2023-05-04
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器械摘要
常见问题
What is the Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C?
Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C is a medical device that received FDA 510(k) clearance on 2023-05-04. The listed applicant is Nucleix , Ltd.. The 510(k) number is K203245.
When did Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C receive FDA 510(k) clearance?
Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C received FDA 510(k) clearance on 2023-05-04, under 510(k) number K203245.
Who is the listed applicant for Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C?
The FDA 510(k) record lists Nucleix , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C?
The FDA product code for Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C is MMW.
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