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 generator, electronic noise (for audiometric testing)
510(k) Number K771188
Device Name REVERSING CLICK GENERATOR RCG6
Applicant
TECA, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
TECA, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number874.1120
Classification Product Code
ETS  
Date Received07/01/1977
Decision Date 07/14/1977
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
-
-