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FIBERLASE C02 LASER WAVEGUIDE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100384
510(k) Type
Special
Applicant
LUMENIS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/12/2010
Days to Decision
55 days
Submission Type
Summary

FIBERLASE C02 LASER WAVEGUIDE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100384
510(k) Type
Special
Applicant
LUMENIS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/12/2010
Days to Decision
55 days
Submission Type
Summary