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 X-Ray, Tomography, Computed, Dental
510(k) Number K190496
Device Name hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
Applicant
CEFLA S.C.
Via Selice Provinciale 23/A
Imola,  IT 40026
Applicant Contact Elena Arcangeli
Correspondent
CEFLA S.C.
Via Selice Provinciale 23/A
Imola,  IT 40026
Correspondent Contact Elena Arcangeli
Regulation Number892.1750
Classification Product Code
OAS  
Subsequent Product Code
MUH  
Date Received02/28/2019
Decision Date 04/24/2019
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
-
-