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
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name lubricant, personal
510(k) Number K060098
Device Name DUREX PLAY TEMPTATIONS ASSORTED LUBRICANTS
Applicant
SSL AMERICAS, INC.
3585 ENGINEERING DR.
SUITE 200
NORCROSS,  GA  30092
Applicant Contact CHRIS ROBINSON
Correspondent
SSL AMERICAS, INC.
3585 ENGINEERING DR.
SUITE 200
NORCROSS,  GA  30092
Correspondent Contact CHRIS ROBINSON
Regulation Number884.5300
Classification Product Code
NUC  
Date Received01/13/2006
Decision Date 06/08/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-