FDA 510(k), K192719, Osom Ultra Plus Flu A&B Test Kit

FDA 510(k), K192719, Osom Ultra Plus Flu A&B Test Kit

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510(K) Number: K192719
Device Name: Osom Ultra Plus Flu A&B Test Kit
Manufacturer: Nisha Li
Device Classification Name: Devices Detecting Influenza A, B, And C Virus Antigens
Regulation Number: PSZ
Classification Product Code: 09/26/2019
Date Received: 04/03/2020
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Microbiology

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