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 K092730
Device Name COSMEDENT BRUSHABLE COMPOSITE
Applicant
Cosmedent, Inc.
401 N. Michigan Ave. Suite 2500
Chicago,  IL  60611
Applicant Contact JAMES L SANDRIK
Correspondent
Cosmedent, Inc.
401 N. Michigan Ave. Suite 2500
Chicago,  IL  60611
Correspondent Contact JAMES L SANDRIK
Regulation Number872.3690
Classification Product Code
EBF  
Date Received09/04/2009
Decision Date 11/20/2009
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-