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MEDILASER, MODEL 1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063745
510(k) Type
Traditional
Applicant
LASER THERA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2007
Days to Decision
125 days
Submission Type
Summary

MEDILASER, MODEL 1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063745
510(k) Type
Traditional
Applicant
LASER THERA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2007
Days to Decision
125 days
Submission Type
Summary