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 tester, auditory impedance
510(k) Number K924934
Device Name AUTOMATIC IMPEDANCE METER AE-205
Applicant
AMERICAN ELECTROMEDICS CORP.
13 COLUMBUS DR.
SUITE 18
AMHERST,  NH  03031
Applicant Contact GLEASON
Correspondent
AMERICAN ELECTROMEDICS CORP.
13 COLUMBUS DR.
SUITE 18
AMHERST,  NH  03031
Correspondent Contact GLEASON
Regulation Number874.1090
Classification Product Code
ETY  
Date Received09/30/1992
Decision Date 01/21/1993
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
-
-