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LASERPRO 810, 940 AND 980 DIODE LASER SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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