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MULTILASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123777
510(k) Type
Traditional
Applicant
Ultralight Laser Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2013
Days to Decision
122 days
Submission Type
Summary

MULTILASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123777
510(k) Type
Traditional
Applicant
Ultralight Laser Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2013
Days to Decision
122 days
Submission Type
Summary