Last synced on 25 January 2026 at 3:41 am

NOVUS TTX LASER AND DELIVERY DEVICES WITH ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032357
510(k) Type
Traditional
Applicant
Lumenis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2003
Days to Decision
71 days
Submission Type
Summary

NOVUS TTX LASER AND DELIVERY DEVICES WITH ACCESSORIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032357
510(k) Type
Traditional
Applicant
Lumenis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2003
Days to Decision
71 days
Submission Type
Summary