FDA 510(k) Applications Submitted by JAMIESON FILM CO.

FDA 510(k) Number Submission Date Device Name Applicant
K960043 01/03/1996 KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM JAMIESON FILM CO.
K970738 02/28/1997 KODAK DIGITAL SCIENCE CARDIAC DIGITAL ACQUISITION UNIT JAMIESON FILM CO.
K971128 03/27/1997 CAP-35B III/CINE 275 JAMIESON FILM CO.
K963334 08/26/1996 JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 JAMIESON FILM CO.


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