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 K963063
Device Name SNORE TEC
Applicant
MARKETING TECHNOLOGIES, INC.
4000 STOCKDALE HWY., STE. H
BAKERSFIELD,  CA  93309
Applicant Contact THOMAS D HALL
Correspondent
MARKETING TECHNOLOGIES, INC.
4000 STOCKDALE HWY., STE. H
BAKERSFIELD,  CA  93309
Correspondent Contact THOMAS D HALL
Regulation Number872.5570
Classification Product Code
LRK  
Date Received08/07/1996
Decision Date 04/14/1997
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
-
-