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LUMENIS VERSAPULSE POWERSUITE HOLMIUM (HO:YAG) AND DUAL WAVELENGTH (HO:YAG/ND:YAG) SURGICAL LASERS AND DELIVERY DEVICES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011703
510(k) Type
Traditional
Applicant
Lumenis
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2001
Days to Decision
89 days
Submission Type
Summary

LUMENIS VERSAPULSE POWERSUITE HOLMIUM (HO:YAG) AND DUAL WAVELENGTH (HO:YAG/ND:YAG) SURGICAL LASERS AND DELIVERY DEVICES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011703
510(k) Type
Traditional
Applicant
Lumenis
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2001
Days to Decision
89 days
Submission Type
Summary