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 Crown And Bridge, Temporary, Resin
510(k) Number K941849
Device Name PROVIPONT C&B
Applicant
Ivoclar USA, Inc.
175 Pineview Dr.
Amherst,  NY  14150
Applicant Contact LLOYD V ZIEMENDORF
Correspondent
Ivoclar USA, Inc.
175 Pineview Dr.
Amherst,  NY  14150
Correspondent Contact LLOYD V ZIEMENDORF
Regulation Number872.3770
Classification Product Code
EBG  
Date Received04/14/1994
Decision Date 08/17/1994
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
-
-