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IMALUX OCT PROBE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K041077
510(k) Type
Traditional
Applicant
IMALUX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2004
Days to Decision
60 days
Submission Type
Summary

IMALUX OCT PROBE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K041077
510(k) Type
Traditional
Applicant
IMALUX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2004
Days to Decision
60 days
Submission Type
Summary