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AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180597
510(k) Type
Special
Applicant
Lumenis Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/3/2018
Days to Decision
28 days
Submission Type
Summary

AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180597
510(k) Type
Special
Applicant
Lumenis Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/3/2018
Days to Decision
28 days
Submission Type
Summary