• 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 Alloy, Gold-Based Noble Metal
510(k) Number K960256
Device Name DEGUDENT LS
Applicant
Degussa Corp.
3950 S. Clinton Ave.
South Plainfield,  NJ  07080
Applicant Contact HOLGER MEINICKE
Correspondent
Degussa Corp.
3950 S. Clinton Ave.
South Plainfield,  NJ  07080
Correspondent Contact HOLGER MEINICKE
Regulation Number872.3060
Classification Product Code
EJT  
Date Received01/18/1996
Decision Date 02/21/1996
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
-
-