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 Adjunctive Cardiac Amyloidosis Status Indicator
510(k) Number K240860
Device Name EchoGo Amyloidosis (1.0)
Applicant
Ultromics Limited
4630 Kingsgate
Cascade Way, Oxford Business Park
Oxford,  GB OX4 2SU
Applicant Contact Jaco Jacobs
Correspondent
Ultromics Limited
4630 Kingsgate
Cascade Way, Oxford Business Park
Oxford,  GB OX4 2SU
Correspondent Contact Jaco Jacobs
Regulation Number870.2200
Classification Product Code
SDJ  
Date Received03/28/2024
Decision Date 11/15/2024
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-