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 Pad, Menstrual, Unscented
510(k) Number K862270
Device Name LAURIER OVERNIGHT SANITARY NAPKIN (MODIFICATION)
Applicant
KAO CORP.
14-10, NIHONBASHI KAYABACHO
1-CHOME, CHUO-KU
TOKYO 103 JAPAN,  JP
Applicant Contact KAZAMA, PH.D.
Correspondent
KAO CORP.
14-10, NIHONBASHI KAYABACHO
1-CHOME, CHUO-KU
TOKYO 103 JAPAN,  JP
Correspondent Contact KAZAMA, PH.D.
Regulation Number884.5435
Classification Product Code
HHD  
Date Received06/13/1986
Decision Date 07/07/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-