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CANDELA SPTL PULSED DYE LASERS

Page Type
Cleared 510(K)
510(k) Number
K931762
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1994
Days to Decision
341 days
Submission Type
Summary

CANDELA SPTL PULSED DYE LASERS

Page Type
Cleared 510(K)
510(k) Number
K931762
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1994
Days to Decision
341 days
Submission Type
Summary