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CANDELA SCLERO LONG PULSE LASER (AKA VBEAM)

Page Type
Cleared 510(K)
510(k) Number
K013748
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2002
Days to Decision
90 days
Submission Type
Summary

CANDELA SCLERO LONG PULSE LASER (AKA VBEAM)

Page Type
Cleared 510(K)
510(k) Number
K013748
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2002
Days to Decision
90 days
Submission Type
Summary