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 Device, Jaw Repositioning
510(k) Number K880956
Device Name SNOAR(TM) OPEN AIRWAY APPLIANCE
Applicant
Kent J. Toone, D.D.S.
10301 S. De Anza Blvd.
Suite 4
Cupertino,  CA  95014
Applicant Contact KENT J TOONE,D.D.S.
Correspondent
Kent J. Toone, D.D.S.
10301 S. De Anza Blvd.
Suite 4
Cupertino,  CA  95014
Correspondent Contact KENT J TOONE,D.D.S.
Regulation Number872.5570
Classification Product Code
LQZ  
Date Received03/07/1988
Decision Date 05/11/1988
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
-
-