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LUMENIS FAMILY OF ULTRAPULSE SURGITOUCH CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
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)
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