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FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022228
510(k) Type
Traditional
Applicant
Iridex Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2002
Days to Decision
90 days
Submission Type
Summary

FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022228
510(k) Type
Traditional
Applicant
Iridex Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2002
Days to Decision
90 days
Submission Type
Summary