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 Burnisher, Operative
510(k) Number K896565
Device Name DMV(R) VENEER SUCTION GRIPPER
Applicant
Dmv Corp.
P.O. Box 878
Zanesville,  OH  43702
Applicant Contact ROBERT C ENGLAND
Correspondent
Dmv Corp.
P.O. Box 878
Zanesville,  OH  43702
Correspondent Contact ROBERT C ENGLAND
Regulation Number872.4565
Classification Product Code
EKJ  
Date Received11/17/1989
Decision Date 02/02/1990
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
-
-