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LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121471
510(k) Type
Traditional
Applicant
Lightscalpel, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2012
Days to Decision
53 days
Submission Type
Summary

LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121471
510(k) Type
Traditional
Applicant
Lightscalpel, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2012
Days to Decision
53 days
Submission Type
Summary