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LightScalpel

Page Type
Cleared 510(K)
510(k) Number
K173827
510(k) Type
Traditional
Applicant
LightScalpel LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2018
Days to Decision
270 days
Submission Type
Summary

LightScalpel

Page Type
Cleared 510(K)
510(k) Number
K173827
510(k) Type
Traditional
Applicant
LightScalpel LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2018
Days to Decision
270 days
Submission Type
Summary