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 Material, Tooth Shade, Resin
510(k) Number K970683
Device Name ZENTIH FLOWABLE COMPOSITE (MULTIPLE)
Applicant
Foremost Dental Mfg., Inc.
242 - S. Dean St.
Englewood,  NJ  07631
Applicant Contact D.T. WOLF
Correspondent
Foremost Dental Mfg., Inc.
242 - S. Dean St.
Englewood,  NJ  07631
Correspondent Contact D.T. WOLF
Regulation Number872.3690
Classification Product Code
EBF  
Date Received02/24/1997
Decision Date 07/15/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-