• 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 K170551
Device Name ImPACT Quick Test
Applicant
ImPACT Applications, Inc.
9665 Granite Ridge Drive, Suite 550
san diego,  CA  92123
Applicant Contact michael zagorski
Correspondent
ImPACT Applications, Inc.
9665 Granite Ridge Drive, Suite 550
san diego,  CA  92123
Correspondent Contact michael zagorski
Regulation Number882.1471
Classification Product Code
POM  
Date Received02/24/2017
Decision Date 06/21/2017
Decision substantially equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
summary summary
Type Traditional
Clinical Trials NCT02597504
Reviewed by Third Party No
Combination Product No
-
-