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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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