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 Automated Radiological Image Processing Software
510(k) Number K231324
Device Name DASI Dimensions (V1.0)
Applicant
DASI Simulations
5115 Parkcenter Ave
Suite 205
Dublin,  OH  43017
Applicant Contact Sri Krishna Sivakumar
Correspondent
DASI Simulations
5115 Parkcenter Ave
Suite 205
Dublin,  OH  43017
Correspondent Contact Lakshmi Dasi
Regulation Number892.2050
Classification Product Code
QIH  
Date Received05/08/2023
Decision Date 01/08/2024
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-