• 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 locator, root apex
510(k) Number K921979
Device Name ROOT ZX
Applicant
J. MORITA USA, INC.
9 MASON
IRVINE,  CA  92618
Applicant Contact RONALD D NEWMAN
Correspondent
J. MORITA USA, INC.
9 MASON
IRVINE,  CA  92618
Correspondent Contact RONALD D NEWMAN
Classification Product Code
LQY  
Date Received04/28/1992
Decision Date 05/27/1993
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-