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IRIDEX OCULIGHT TX

Page Type
Cleared 510(K)
510(k) Number
K062369
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2006
Days to Decision
86 days
Submission Type
Summary

IRIDEX OCULIGHT TX

Page Type
Cleared 510(K)
510(k) Number
K062369
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2006
Days to Decision
86 days
Submission Type
Summary