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FIATLUX VISUALIZE

Page Type
Cleared 510(K)
510(k) Number
K082041
510(k) Type
Traditional
Applicant
FIATLUX IMAGING INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2008
Days to Decision
14 days
Submission Type
Summary

FIATLUX VISUALIZE

Page Type
Cleared 510(K)
510(k) Number
K082041
510(k) Type
Traditional
Applicant
FIATLUX IMAGING INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2008
Days to Decision
14 days
Submission Type
Summary