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LUMENIS FAMILY OF ULTRAPULSE SURGITOUCH CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030147
510(k) Type
Traditional
Applicant
LUMENIS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2003
Days to Decision
90 days
Submission Type
Summary

LUMENIS FAMILY OF ULTRAPULSE SURGITOUCH CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030147
510(k) Type
Traditional
Applicant
LUMENIS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2003
Days to Decision
90 days
Submission Type
Summary