510(k) K183059

3nethra neo by Forus Health Pvt.Ltd — Product Code HKI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 21, 2018
Date Received
November 2, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Camera, Ophthalmic, Ac-Powered
Device Class
Class II
Regulation Number
886.1120
Review Panel
OP
Submission Type