• 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 Hearing Aid, Master
510(k) Number K964080
Device Name LORI HEARING AID SIMULATOR
Applicant
LORI MEDICAL LABORATORIES, INC.
696 MENDELSSOHN AVE. NORTH
GOLDEN VALLEY,  MN  55427 -4306
Applicant Contact GARY R MAAS
Correspondent
LORI MEDICAL LABORATORIES, INC.
696 MENDELSSOHN AVE. NORTH
GOLDEN VALLEY,  MN  55427 -4306
Correspondent Contact GARY R MAAS
Regulation Number874.3330
Classification Product Code
KHL  
Date Received10/11/1996
Decision Date 01/08/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-