Last synced on 14 November 2025 at 11:06 pm

VERSAPULSE MODEL P20 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100228
510(k) Type
Special
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2010
Days to Decision
29 days
Submission Type
Summary

VERSAPULSE MODEL P20 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100228
510(k) Type
Special
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2010
Days to Decision
29 days
Submission Type
Summary