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 System, Nuclear Magnetic Resonance Imaging
510(k) Number K254250
Device Name MagicScan-1.5, GreenMR Serenity 1.5T
Applicant
Xingaoyi Medical Equipment Co.,Ltd
#555 Yeshan Rd.
Yuyao,  CN
Applicant Contact ZhengYing ZUO
Correspondent
Xingaoyi Medical Equipment Co.,Ltd
#555 Yeshan Rd.
Yuyao,  CN
Correspondent Contact ZhengYing ZUO
Regulation Number892.1000
Classification Product Code
LNH  
Date Received12/29/2025
Decision Date 08/17/2026
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
-
-