Last synced on 14 November 2025 at 11:06 pm

LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980

Page Type
Cleared 510(K)
510(k) Number
K040294
510(k) Type
Traditional
Applicant
PHOTOMEDEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2004
Days to Decision
89 days
Submission Type
Summary

LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980

Page Type
Cleared 510(K)
510(k) Number
K040294
510(k) Type
Traditional
Applicant
PHOTOMEDEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2004
Days to Decision
89 days
Submission Type
Summary