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 K930576
Device Name AT42
Applicant
AUTOJECT SYSTEMS, INC.
OAKWOOD CENTRE
620 WHEAT LANE
OAK DALE,  IL  60191
Applicant Contact SAID EL-DINARY
Correspondent
AUTOJECT SYSTEMS, INC.
OAKWOOD CENTRE
620 WHEAT LANE
OAK DALE,  IL  60191
Correspondent Contact SAID EL-DINARY
Regulation Number882.5050
Classification Product Code
HCC  
Date Received02/04/1993
Decision Date 05/18/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-