Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EyeQ nanoECP

K-Number: K243014 · 2025-06-18

ApplicantEyeq, Inc.
Decision Date2025-06-18
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EyeQ nanoECP is a medical device manufactured by Eyeq, Inc.. It received FDA 510(k) clearance on 2025-06-18 under approval number K243014. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EyeQ nanoECP?

EyeQ nanoECP is a medical device that received FDA 510(k) clearance on 2025-06-18. It is manufactured by Eyeq, Inc.. The 510(k) number is K243014.

When was EyeQ nanoECP approved by the FDA?

EyeQ nanoECP received FDA 510(k) clearance on 2025-06-18, under approval number K243014.

What company makes EyeQ nanoECP?

EyeQ nanoECP is manufactured by Eyeq, Inc..

What is the FDA product code for EyeQ nanoECP?

The FDA product code for EyeQ nanoECP is HQF.

Related Devices (Code: HQF)

K153769R:GEN Laser SystemLutronic Corporation K152688LightLas Multi-Wavelength Medical Laser SystemLightmed Corporation K152603Green Laser Photocoagulator GYC-500Nidek Co., Ltd. K171488PSLT for PASCAL StreamlineTopcon Medical Laser Systems, Inc. K170067EasyretQuantel Medical K170302YELLOW LASER PHOTOCOAGULATOR YLC-500Nidek Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑