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The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories

Page Type
Cleared 510(K)
510(k) Number
K220467
510(k) Type
Traditional
Applicant
Lumenis Be, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
5/18/2022
Days to Decision
90 days
Submission Type
Summary

The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories

Page Type
Cleared 510(K)
510(k) Number
K220467
510(k) Type
Traditional
Applicant
Lumenis Be, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
5/18/2022
Days to Decision
90 days
Submission Type
Summary