Last synced on 25 April 2025 at 11:05 pm

NOVUS 3000 LASER SYSTEM AND DELIVERY DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052526
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2005
Days to Decision
62 days
Submission Type
Summary

NOVUS 3000 LASER SYSTEM AND DELIVERY DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052526
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2005
Days to Decision
62 days
Submission Type
Summary