• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Device Classification Under Section 513(f)(2)(De Novo)

  • 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 device, detection, sulfide
De Novo Number DEN980003
510(K) Number K980749
Device Name DIAMOND PROBE/PERIO 2000 SYSTEM
Requester
DIAMOND GENERAL DEVELOPMENT CORP.
333 parkland plaza
ann arbor,  MI  48103
Contact dale e seamon
Regulation Number872.1870
Classification Product Code
MVH  
Date Received05/18/1998
Decision Date 07/17/1998
Decision granted (DENG)
Classification Advisory Committee Dental
Review Advisory Committee Dental
Reclassification Order Reclassification Order
Type Post-NSE
-
-