• 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, Gamete, Fertilization, And Embryo Compatible
510(k) Number K072741
FOIA Releasable 510(k) K072741
Device Name PRE-VA VAGINAL LUBRICANT
Applicant
INGFERTILITY, LLC
17206 S. SPANGLE CREEK RD.
VALLEYFORD,  WA  99036
Applicant Contact DENNIS CLIFTON
Correspondent
INGFERTILITY, LLC
17206 S. SPANGLE CREEK RD.
VALLEYFORD,  WA  99036
Correspondent Contact DENNIS CLIFTON
Regulation Number884.5300
Classification Product Code
PEB  
Date Received09/27/2007
Decision Date 07/16/2008
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
-
-