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 Electromyograph, Diagnostic
510(k) Number K802637
Device Name TECA MODEL-10 ELECTROMYOGRAPH
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 Number890.1375
Classification Product Code
IKN  
Date Received10/22/1980
Decision Date 11/26/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-