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LightForce LTS Model 1000, 1500, 2500, and 4000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173067
510(k) Type
Traditional
Applicant
LiteCure, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2018
Days to Decision
146 days
Submission Type
Summary

LightForce LTS Model 1000, 1500, 2500, and 4000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173067
510(k) Type
Traditional
Applicant
LiteCure, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2018
Days to Decision
146 days
Submission Type
Summary