• 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, Scented
510(k) Number K864673
Device Name UNSCENTED MENSTRUAL PAD
Applicant
PROCTER & GAMBLE MFG. CO.
P.O. BOX 599
CINCINNATI,  OH  45201
Applicant Contact JAMES T O'REILLY
Correspondent
PROCTER & GAMBLE MFG. CO.
P.O. BOX 599
CINCINNATI,  OH  45201
Correspondent Contact JAMES T O'REILLY
Regulation Number884.5425
Classification Product Code
HHL  
Date Received12/02/1986
Decision Date 01/21/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-