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CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081324
510(k) Type
Special
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
36 days
Submission Type
Summary

CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081324
510(k) Type
Special
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
36 days
Submission Type
Summary