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CANDELA FAMILY OF PULSED DYE LASER SYSTEMS: PIGMENTED LESION HANDPIECE ACCESSORY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051359
510(k) Type
Traditional
Applicant
Candela Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2005
Days to Decision
50 days
Submission Type
Summary

CANDELA FAMILY OF PULSED DYE LASER SYSTEMS: PIGMENTED LESION HANDPIECE ACCESSORY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051359
510(k) Type
Traditional
Applicant
Candela Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2005
Days to Decision
50 days
Submission Type
Summary