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The UltraPulse system (UltraPulse and UltraPulse DUO models,members of the modified Lumenis Family of UltraPulse SurgiTouch

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151331
510(k) Type
Special
Applicant
LUMENIS LTD
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/30/2015
Days to Decision
42 days
Submission Type
Summary

The UltraPulse system (UltraPulse and UltraPulse DUO models,members of the modified Lumenis Family of UltraPulse SurgiTouch

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151331
510(k) Type
Special
Applicant
LUMENIS LTD
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/30/2015
Days to Decision
42 days
Submission Type
Summary