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Fundus On Phone Non Mydriatic (FOP NM-10)

K252120 Class II Traditional
Decision Date
2025-12-12
Sponsor / Applicant
Remidio Innovative Solutions Private Limited

Technical Specification

510(k) Submission ID K252120
Product Code HKI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1120
Decision Date 2025-12-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Fundus On Phone Non Mydriatic (FOP NM-10) received FDA 510(k) clearance under submission number K252120, sponsored by Remidio Innovative Solutions Private Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2025-12-12.

Classification & Regulation

This clearance is catalogued under FDA product code HKI and 21 CFR 886.1120, within the Ophthalmic review panel as a Class II device.