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, anti-snoring
510(k) Number K020893
Device Name NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE
Applicant
DENNIS R. BAILEY, DDS
7901 EAST BELLEVIEW AVE.
SUITE 200
ENGLEWOOD,  CO  80111
Applicant Contact DENNIS R BAILEY
Correspondent
DENNIS R. BAILEY, DDS
7901 EAST BELLEVIEW AVE.
SUITE 200
ENGLEWOOD,  CO  80111
Correspondent Contact DENNIS R BAILEY
Regulation Number872.5570
Classification Product Code
LRK  
Date Received03/19/2002
Decision Date 05/28/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-