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CANDELA CLEARBEAM PULSED DYE LASER

Page Type
Cleared 510(K)
510(k) Number
K013043
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2001
Days to Decision
31 days
Submission Type
Summary

CANDELA CLEARBEAM PULSED DYE LASER

Page Type
Cleared 510(K)
510(k) Number
K013043
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2001
Days to Decision
31 days
Submission Type
Summary