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 Cleanser, Root Canal
510(k) Number K992919
Device Name OXY-GLIDE ROOT CANAL CLEANSER & LUB.
Applicant
SUPER GLIDE, INC.
227 COLCHESTER AVE.
BURLINGTON,  VT  05401
Applicant Contact VICTOR L RATKUS
Correspondent
SUPER GLIDE, INC.
227 COLCHESTER AVE.
BURLINGTON,  VT  05401
Correspondent Contact VICTOR L RATKUS
Classification Product Code
KJJ  
Date Received08/30/1999
Decision Date 11/19/1999
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-