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VIRIDIS DERMA LASER

Page Type
Cleared 510(K)
510(k) Number
K020071
510(k) Type
Traditional
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2002
Days to Decision
86 days
Submission Type
Summary

VIRIDIS DERMA LASER

Page Type
Cleared 510(K)
510(k) Number
K020071
510(k) Type
Traditional
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2002
Days to Decision
86 days
Submission Type
Summary