• 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 K171021
Device Name JO Agapé Personal Lubricant
Applicant
United Consortium
29000 N. Hancock Pkwy
Valencia,  CA  91355
Applicant Contact Stephanie Morris
Correspondent
United Consortium
29000 N. Hancock Pkwy
Valencia,  CA  91355
Correspondent Contact Stephanie Morris
Regulation Number884.5300
Classification Product Code
NUC  
Date Received04/05/2017
Decision Date 07/18/2017
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
-
-