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CANDELA GENTLELASE II DERMATOLOGICAL LASER

Page Type
Cleared 510(K)
510(k) Number
K984601
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1999
Days to Decision
38 days
Submission Type
Summary

CANDELA GENTLELASE II DERMATOLOGICAL LASER

Page Type
Cleared 510(K)
510(k) Number
K984601
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1999
Days to Decision
38 days
Submission Type
Summary