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 Alloy, Metal, Base
510(k) Number K905034
Device Name HD-4 CROWN & BRIDGE ALLOY
Applicant
Ho Dental Co., Inc.
P.O. Box 143
2723 Hawthorn Ln.
Wilmette,  IL  60091
Applicant Contact DAVID HOLZMANN
Correspondent
Ho Dental Co., Inc.
P.O. Box 143
2723 Hawthorn Ln.
Wilmette,  IL  60091
Correspondent Contact DAVID HOLZMANN
Regulation Number872.3710
Classification Product Code
EJH  
Date Received11/07/1990
Decision Date 09/05/1991
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
-
-