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LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
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)
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