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 Attachment, Precision, All
510(k) Number K900785
Device Name MICRO 2 SYSTEM
Applicant
Inodent
Suite 120 Canal Square
1054 31st St. NW
Washington,  DC  20007
Applicant Contact JEAN-PIERRE LACLAU
Correspondent
Inodent
Suite 120 Canal Square
1054 31st St. NW
Washington,  DC  20007
Correspondent Contact JEAN-PIERRE LACLAU
Regulation Number872.3165
Classification Product Code
EGG  
Date Received02/20/1990
Decision Date 04/16/1990
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
-
-