• 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 adhesive, denture, polyvinyl methylether maleic acid calcium-sodium double salt
510(k) Number K862876
Device Name NEW SUPER POLI-GRIP DENTURE ADHESIVE CREAM
Applicant
BLOCK DRUG COMPANY, INC.
257 CORNELISON AVE.
JERSEY CITY,  NJ  07302
Applicant Contact HOWARD FEINMAN
Correspondent
BLOCK DRUG COMPANY, INC.
257 CORNELISON AVE.
JERSEY CITY,  NJ  07302
Correspondent Contact HOWARD FEINMAN
Regulation Number872.3490
Classification Product Code
KOO  
Date Received07/30/1986
Decision Date 08/29/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-