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APEX 800 LASER SYSTEM, MODEL APEX 800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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