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CANDELA GENTLELASE FAMILY OF LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K024335
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2003
Days to Decision
75 days
Submission Type
Summary

CANDELA GENTLELASE FAMILY OF LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K024335
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2003
Days to Decision
75 days
Submission Type
Summary