FDA 510(k)

EyeQ nanoECP

K-Number: K243014 · 2025-06-18

Decision Date2025-06-18

Product CodeHQF

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

EyeQ nanoECP is the device name listed in this FDA 510(k) record. The listed applicant is Eyeq, Inc.. It received FDA 510(k) clearance on 2025-06-18 under 510(k) 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. The listed applicant is Eyeq, Inc.. The 510(k) number is K243014.

When did EyeQ nanoECP receive FDA 510(k) clearance?

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

Who is the listed applicant for EyeQ nanoECP?

The FDA 510(k) record lists Eyeq, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EyeQ nanoECP?

The FDA product code for EyeQ nanoECP is HQF.

Related Devices (Code: HQF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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