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LUMALITE CURE LIGHT, MODEL 2100

Page Type
Cleared 510(K)
510(k) Number
K002566
510(k) Type
Traditional
Applicant
LUMALITE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2000
Days to Decision
63 days
Submission Type
Summary

LUMALITE CURE LIGHT, MODEL 2100

Page Type
Cleared 510(K)
510(k) Number
K002566
510(k) Type
Traditional
Applicant
LUMALITE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2000
Days to Decision
63 days
Submission Type
Summary