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PLTL-1 & PLDL-1 510NM PULSED DYE LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934811
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1994
Days to Decision
329 days
Submission Type
Summary

PLTL-1 & PLDL-1 510NM PULSED DYE LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934811
510(k) Type
Traditional
Applicant
CANDELA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1994
Days to Decision
329 days
Submission Type
Summary