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FAMILI OF IRIDEX IQ LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K071687
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2008
Days to Decision
416 days
Submission Type
Summary

FAMILI OF IRIDEX IQ LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K071687
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2008
Days to Decision
416 days
Submission Type
Summary