• 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 Material, Impression
510(k) Number K935888
Device Name ELITE FAST LIGHT BODY
Applicant
Zhermack Dental Production
Via Bovazecchino, 100
45021 Badia Polesine
(Rovigo) Italy,  IT
Applicant Contact MONICA MARTELLO
Correspondent
Zhermack Dental Production
Via Bovazecchino, 100
45021 Badia Polesine
(Rovigo) Italy,  IT
Correspondent Contact MONICA MARTELLO
Regulation Number872.3660
Classification Product Code
ELW  
Date Received10/12/1993
Decision Date 08/23/1994
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
-
-