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LASERPRO 810, 940 AND 980 DIODE LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K082721
510(k) Type
Traditional
Applicant
PHOTOMEDEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2008
Days to Decision
41 days
Submission Type
Summary

LASERPRO 810, 940 AND 980 DIODE LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K082721
510(k) Type
Traditional
Applicant
PHOTOMEDEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2008
Days to Decision
41 days
Submission Type
Summary