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 K932932
Device Name SNOREMASTER SNORE REMEDY
Applicant
The Snoremaster Co.
3530 Henry Ave.
Philadelphia,  PA  19129
Applicant Contact LEROY S FORNEY
Correspondent
The Snoremaster Co.
3530 Henry Ave.
Philadelphia,  PA  19129
Correspondent Contact LEROY S FORNEY
Regulation Number872.5570
Classification Product Code
LQZ  
Date Received06/16/1993
Decision Date 02/10/1995
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
-
-