• 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 system, image processing, radiological
510(k) Number K173939
Device Name Quantib Brain
Applicant
Quantib BV
Westblaak 106
rotterdam,  NL 3012 km
Applicant Contact floor van leeuwen
Correspondent
Quantib BV
Westblaak 106
rotterdam,  NL 3012 km
Correspondent Contact floor van leeuwen
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received12/26/2017
Decision Date 03/09/2018
Decision substantially equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-