• 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 Bur, Dental
510(k) Number K863097
Device Name CB BUR
Applicant
Beavers Dental, Div. Sybron Canada, Ltd.
Nixon,Hargrave,Devans & Doyle
Suite 800, One Thomas Circle
Washington,  DC  20005
Applicant Contact STEPHEN KURZMAN
Correspondent
Beavers Dental, Div. Sybron Canada, Ltd.
Nixon,Hargrave,Devans & Doyle
Suite 800, One Thomas Circle
Washington,  DC  20005
Correspondent Contact STEPHEN KURZMAN
Regulation Number872.3240
Classification Product Code
EJL  
Date Received08/14/1986
Decision Date 08/26/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-