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, Test, Immunological, Antigen, Tumor
510(k) Number K964407
Device Name IMX CA 15-3
Applicant
Abbott Laboratories
Dept. 389, Ap30
200 Abbott Park Rd.
Abbott Park,  IL  60064 -3537
Applicant Contact JOY C SONSALLA
Correspondent
Abbott Laboratories
Dept. 389, Ap30
200 Abbott Park Rd.
Abbott Park,  IL  60064 -3537
Correspondent Contact JOY C SONSALLA
Regulation Number866.6010
Classification Product Code
MOI  
Date Received11/04/1996
Decision Date 11/10/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Immunology
510k Review Panel Immunology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-