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CANDELA GENTLELASE GL DERMATOLOGICAL VASCULAR LESION LASER

Page Type
Cleared 510(K)
510(k) Number
K972767
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1997
Days to Decision
133 days
Submission Type
Summary

CANDELA GENTLELASE GL DERMATOLOGICAL VASCULAR LESION LASER

Page Type
Cleared 510(K)
510(k) Number
K972767
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1997
Days to Decision
133 days
Submission Type
Summary