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 Wax, Dental, Intraoral
510(k) Number K914513
Device Name PALAVIT G
Applicant
Heraeus Kulzer, Inc.
10005 Muirlands Blvd.
Irvine,  CA  92718
Applicant Contact SHARON PARKER
Correspondent
Heraeus Kulzer, Inc.
10005 Muirlands Blvd.
Irvine,  CA  92718
Correspondent Contact SHARON PARKER
Regulation Number872.6890
Classification Product Code
EGD  
Date Received10/09/1991
Decision Date 03/19/1992
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
-
-