• 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 Computerized Cognitive Assessment Aid For Concussion
510(k) Number K231688
Device Name ImPACT Version 4
Applicant
Impact Applications, Inc.
2140 Norcor Ave., Suite 115
Coralville,  IA  52241
Applicant Contact Michael Zagorski
Correspondent
Impact Applications, Inc.
2140 Norcor Ave., Suite 115
Coralville,  IA  52241
Correspondent Contact Michael Zagorski
Regulation Number882.1471
Classification Product Code
POM  
Date Received06/09/2023
Decision Date 09/16/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-