Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
1 to 3 of 3 Results
ProductCode: GEX Applicant: PHOTOMEDEX, INC Decision Date To: 10/24/2016
Results per Page
New Search  
Export all 3 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
laserpro 810, 940 and 980 diode laser systems PHOTOMEDEX, INC. K082721 10/28/2008
laserpro co2 carbon dioxide laser system PHOTOMEDEX, INC. K040234 04/02/2004
laserpro diode laser systems, models 810, 940 & 980 PHOTOMEDEX, INC. K040294 05/05/2004
-
-