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SMART CO2 (SMART US 20D / ULTRASPEED, SMART CLINIC AND PERIOPULSE) SURGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081181
510(k) Type
Traditional
Applicant
CYNOSURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2008
Days to Decision
10 days
Submission Type
Summary

SMART CO2 (SMART US 20D / ULTRASPEED, SMART CLINIC AND PERIOPULSE) SURGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081181
510(k) Type
Traditional
Applicant
CYNOSURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2008
Days to Decision
10 days
Submission Type
Summary