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DIOMED 15 DIODE LASER

Page Type
Cleared 510(K)
510(k) Number
K012398
510(k) Type
Traditional
Applicant
DIOMED, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2002
Days to Decision
179 days
Submission Type
Summary

DIOMED 15 DIODE LASER

Page Type
Cleared 510(K)
510(k) Number
K012398
510(k) Type
Traditional
Applicant
DIOMED, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2002
Days to Decision
179 days
Submission Type
Summary