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 Processor, Radiographic-Film, Automatic
510(k) Number K002640
Device Name FREEDOM AUTOMATIC FILM PROCESSOR
Applicant
J. Morita USA, Inc.
9 Mason
Irvine,  CA  92618
Applicant Contact VICTOR MAZZANTI
Correspondent
J. Morita USA, Inc.
9 Mason
Irvine,  CA  92618
Correspondent Contact VICTOR MAZZANTI
Regulation Number892.1900
Classification Product Code
IXW  
Date Received08/24/2000
Decision Date 11/08/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Abbreviated
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-