• 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 pad, menstrual, unscented
510(k) Number K811766
Device Name CONFI-DRY ADULT UROABSORBENT PADS
Applicant
PERSONAL PRODUCTS CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
PERSONAL PRODUCTS CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number884.5435
Classification Product Code
HHD  
Date Received06/22/1981
Decision Date 07/10/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-