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 Airbrush
510(k) Number K964059
Device Name MICADENT
Applicant
Hampton Research
2670 W. Interstate 40
Oklahoma City,  OK  73108
Applicant Contact WILLIAM H HARRIS, DDS
Correspondent
Hampton Research
2670 W. Interstate 40
Oklahoma City,  OK  73108
Correspondent Contact WILLIAM H HARRIS, DDS
Regulation Number872.6080
Classification Product Code
KOJ  
Date Received10/09/1996
Decision Date 12/19/1996
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
-
-