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 Varnish, Cavity
510(k) Number K200614
Device Name FiteBac Antimicrobial Cavity Cleanser
Applicant
Largent Health, LLC
3698 Largent Way NW, Suite 101
Marietta,  GA  30064
Applicant Contact Kirk Kimmerling
Correspondent
Secure Biomed Evalutations
7828 Hickory Flat Highway Suite 120
Woodstock,  GA  30188
Correspondent Contact Elizabeth O’Keeffe
Regulation Number872.3260
Classification Product Code
LBH  
Date Received03/09/2020
Decision Date 06/25/2020
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product Yes
Predetermined Change
Control Plan Authorized		 No
-
-