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 Device, Biofeedback
510(k) Number K842023
Device Name TEMP. & GSR BIOFEEDBACK DEVICE
Applicant
ELECTRONICS RESEARCH & PRODUCTION
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
ELECTRONICS RESEARCH & PRODUCTION
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number882.5050
Classification Product Code
HCC  
Date Received05/18/1984
Decision Date 07/20/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-