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 Hearing Aid, Tactile
510(k) Number K851441
Device Name TACTICON 1600
Applicant
Medecon
21906 Hyannisport
Cupertino,  CA  95014
Applicant Contact EARLE L CANTY
Correspondent
Medecon
21906 Hyannisport
Cupertino,  CA  95014
Correspondent Contact EARLE L CANTY
Classification Product Code
LRA  
Date Received04/10/1985
Decision Date 06/27/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-