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EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS

Page Type
Cleared 510(K)
510(k) Number
K041957
510(k) Type
Traditional
Applicant
DIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2004
Days to Decision
133 days
Submission Type
Summary

EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS

Page Type
Cleared 510(K)
510(k) Number
K041957
510(k) Type
Traditional
Applicant
DIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2004
Days to Decision
133 days
Submission Type
Summary