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CANON Fundus Camera CR-10 (CR-10)

K241049 Class II Special
Decision Date
2024-05-15
Sponsor / Applicant
Canon, Inc.

Technical Specification

510(k) Submission ID K241049
Product Code HKI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1120
Decision Date 2024-05-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CANON Fundus Camera CR-10 (CR-10) received FDA 510(k) clearance under submission number K241049, sponsored by Canon, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2024-05-15.

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.