510(k) K243600

Device
3nethra neo HD FA; 3nethra neo HD
Applicant
Forus Health Pvt.Ltd
510(k) number
K243600
Product code
HKI
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-14
Date received
2024-11-21
Regulation
886.1120
Classification name
Camera, Ophthalmic, Ac-Powered
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
RJ Venkataramanan
Address
# 8, 27th Cross Rd., Banashankari Stage Ii, Banashankari Bengaluru IN 560070 560070

FDA Registration Numbers

Source Documents

510(k) summary PDF

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