• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K190898, Sight OLO, by Sight Diagnostics , Ltd.

FDA 510(k) K190898, Sight OLO, by Sight Diagnostics , Ltd.

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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)
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