FDA 510(k), K190898, Sight OLO

510(K) Number: K190898
Device Name: Sight OLO
Manufacturer: Sight Diagnostics Ltd.
Device Classification Name: Counter, Differential Cell
Regulation Number: 864.5220
Classification Product Code: GKZ
Date Received: 04/05/2019
Decision Date: 11/01/2019
Regulation Medical Specialty: Hematology

86 pages (3,002 of 3,088 original pages are fully redacted)