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 douche apparatus, vaginal, therapeutic
510(k) Number K831667
Device Name FEMININE HYGIENE DEVICE
Applicant
SNOW WILLOW CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SNOW WILLOW CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number884.5900
Classification Product Code
HED  
Date Received05/23/1983
Decision Date 09/12/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-