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Iridex 810 Laser

Page Type
Cleared 510(K)
510(k) Number
K213592
510(k) Type
Special
Applicant
Iridex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2022
Days to Decision
131 days
Submission Type
Summary

Iridex 810 Laser

Page Type
Cleared 510(K)
510(k) Number
K213592
510(k) Type
Special
Applicant
Iridex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2022
Days to Decision
131 days
Submission Type
Summary