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ELITE MPX LASER SYSTEM WITH XPL HANDPIECE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090235
510(k) Type
Traditional
Applicant
CYNOSURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2009
Days to Decision
43 days
Submission Type
Summary

ELITE MPX LASER SYSTEM WITH XPL HANDPIECE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090235
510(k) Type
Traditional
Applicant
CYNOSURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2009
Days to Decision
43 days
Submission Type
Summary