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ULTRApulse Alpha CO2 Laser System, 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
K233301
510(k) Type
Special
Applicant
Lumenis Be Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
63 days
Submission Type
Statement

ULTRApulse Alpha CO2 Laser System, 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
K233301
510(k) Type
Special
Applicant
Lumenis Be Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
63 days
Submission Type
Statement