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IRIDERM, MODEL APEX 800

Page Type
Cleared 510(K)
510(k) Number
K992298
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
154 days
Submission Type
Summary

IRIDERM, MODEL APEX 800

Page Type
Cleared 510(K)
510(k) Number
K992298
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
154 days
Submission Type
Summary