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

FDA 510(k)

MATCHEDFLICKER

K-Number: K090266 · 2009-05-06

ApplicantEyeic Corporation
Decision Date2009-05-06
Product CodeNFJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MATCHEDFLICKER is the device name listed in this FDA 510(k) record. The listed applicant is Eyeic Corporation. It received FDA 510(k) clearance on 2009-05-06 under 510(k) number K090266. The device is classified under product code NFJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATCHEDFLICKER?

MATCHEDFLICKER is a medical device that received FDA 510(k) clearance on 2009-05-06. The listed applicant is Eyeic Corporation. The 510(k) number is K090266.

When did MATCHEDFLICKER receive FDA 510(k) clearance?

MATCHEDFLICKER received FDA 510(k) clearance on 2009-05-06, under 510(k) number K090266.

Who is the listed applicant for MATCHEDFLICKER?

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

What is the FDA product code for MATCHEDFLICKER?

The FDA product code for MATCHEDFLICKER is NFJ.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: NFJ)

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.

K260694ZEISS CLINIC 360Carl Zeiss Meditec, AGK253893Harmony Referral System with Harmony OCT Viewer (Octave)Topcon Healthcare Solutions EMEA OyK234076iCare ALTIUS CWCentervue S.P.A.K232828IMAGEnet6 Ophthalmic Data SystemTopcon CorporationK232944CALLISTO eyeCarl Zeiss Meditec, AGK232555HarmonyTopcon Healthcare Solutions

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.

↑