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LIGHTSCALPEL LS-4020

Page Type
Cleared 510(K)
510(k) Number
K213669
510(k) Type
Traditional
Applicant
LightScalpel Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2023
Days to Decision
450 days
Submission Type
Summary

LIGHTSCALPEL LS-4020

Page Type
Cleared 510(K)
510(k) Number
K213669
510(k) Type
Traditional
Applicant
LightScalpel Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2023
Days to Decision
450 days
Submission Type
Summary