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AcuPulse 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
K212703
510(k) Type
Traditional
Applicant
Lumenis, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/19/2021
Days to Decision
54 days
Submission Type
Summary

AcuPulse 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
K212703
510(k) Type
Traditional
Applicant
Lumenis, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/19/2021
Days to Decision
54 days
Submission Type
Summary