Jamieson Film Co. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Jamieson Film Co. has 6 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 6 cleared submissions from 1991 to 1997. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Jamieson Film Co. Filter by specialty or product code using the sidebar.
6 devices
Cleared
May 07, 1997
KODAK DIGITAL SCIENCE CARDIAC DIGITAL ACQUISITION UNIT
Radiology
68d
Cleared
Apr 28, 1997
CAP-35B III/CINE 275
Radiology
32d
Cleared
Sep 11, 1996
JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100
Radiology
16d
Cleared
Mar 27, 1996
KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM
Radiology
84d
Cleared
Oct 05, 1995
VANGUARD XR-350 CINEANGIOGRAM PROJECTOR
Radiology
66d
Cleared
Sep 24, 1991
JAMIESON JT-CRP CINE FILM PROCESSOR
Radiology
64d