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MODIFIED VERSAPULSE SELECT HO:YAG AND HO:YAG/ND:YAG LASERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980685
510(k) Type
Traditional
Applicant
Lumenis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
86 days
Submission Type
Summary

MODIFIED VERSAPULSE SELECT HO:YAG AND HO:YAG/ND:YAG LASERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980685
510(k) Type
Traditional
Applicant
Lumenis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
86 days
Submission Type
Summary