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 Changer, Radiographic Film/Cassette
510(k) Number K812024
Device Name XEROX 128 CASSETTE CHANGER
Applicant
Xerox Medical Systems
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Xerox Medical Systems
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number892.1860
Classification Product Code
KPX  
Date Received07/20/1981
Decision Date 08/13/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-