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Q-SWITCHED ND:YAG LASER TREATMENT HEAD FOR THE LUMENIS QUANTUM SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043173
510(k) Type
Traditional
Applicant
Lumenis, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2005
Days to Decision
76 days
Submission Type
Summary

Q-SWITCHED ND:YAG LASER TREATMENT HEAD FOR THE LUMENIS QUANTUM SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043173
510(k) Type
Traditional
Applicant
Lumenis, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2005
Days to Decision
76 days
Submission Type
Summary