• 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 Handpiece, Air-Powered, Dental
510(k) Number K901239
Device Name TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE
Applicant
Teledyne Getz
1550 Greenleaf Ave.
Elk Grove Village,  IL  60007
Applicant Contact GABRIEL LEBOVIC
Correspondent
Teledyne Getz
1550 Greenleaf Ave.
Elk Grove Village,  IL  60007
Correspondent Contact GABRIEL LEBOVIC
Regulation Number872.4200
Classification Product Code
EFB  
Date Received03/15/1990
Decision Date 05/15/1990
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
-
-