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K-LASER K-1200, MODEL 12 W

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091497
510(k) Type
Traditional
Applicant
ELTECH, S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2009
Days to Decision
91 days
Submission Type
Summary

K-LASER K-1200, MODEL 12 W

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091497
510(k) Type
Traditional
Applicant
ELTECH, S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2009
Days to Decision
91 days
Submission Type
Summary