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APEX 800 LASER SYSTEM, MODEL APEX 800

Page Type
Cleared 510(K)
510(k) Number
K020849
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2002
Days to Decision
66 days
Submission Type
Summary

APEX 800 LASER SYSTEM, MODEL APEX 800

Page Type
Cleared 510(K)
510(k) Number
K020849
510(k) Type
Traditional
Applicant
IRIDEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2002
Days to Decision
66 days
Submission Type
Summary