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IRIDEX OCULIGHT TX — Iridex Corp (510(k) K062369)

IRIDEX OCULIGHT TX — Iridex Corp (510(k) K062369) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: IRIDEX OCULIGHT TX; Applicant: Iridex Corp; Clearance track: 510(k).

Device nameIRIDEX OCULIGHT TX
ApplicantIridex Corp
Clearance track510(k)
Submission numberK062369
DecisionSubstantially Equivalent
Decision date2006-11-08
Date received2006-08-14
Product codeGEX
Device class2
Medical specialtyGeneral, Plastic Surgery
Applicant locationCA, US
SourceopenFDA device

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