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CANDELA CBEAM PULSED DYE LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K020958
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2002
Days to Decision
88 days
Submission Type
Summary

CANDELA CBEAM PULSED DYE LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K020958
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2002
Days to Decision
88 days
Submission Type
Summary