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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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