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 Powder, Porcelain
510(k) Number K001815
Device Name DC ZIRKON
Applicant
Austenal, Inc.
4101 W. 51st St.
Chicago,  IL  60632 -4287
Applicant Contact RONALD DUDEK
Correspondent
Austenal, Inc.
4101 W. 51st St.
Chicago,  IL  60632 -4287
Correspondent Contact RONALD DUDEK
Regulation Number872.6660
Classification Product Code
EIH  
Date Received06/15/2000
Decision Date 08/10/2000
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
-
-