Last synced on 25 January 2026 at 3:41 am

QUANTUM, MODELS SR, HR, DL; VASCULIGHT, MODELS SR, HR, VS, VX, DL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020839
510(k) Type
Traditional
Applicant
Lumenis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2002
Days to Decision
210 days
Submission Type
Summary

QUANTUM, MODELS SR, HR, DL; VASCULIGHT, MODELS SR, HR, VS, VX, DL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020839
510(k) Type
Traditional
Applicant
Lumenis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2002
Days to Decision
210 days
Submission Type
Summary