Summit Industries, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Summit Industries, Inc. has 6 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 6 cleared submissions from 1985 to 1988. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Summit Industries, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Feb 12, 1988
C900 X-RAY FILM PROCESSOR
Radiology
73d
Cleared
Dec 30, 1987
COLLI-MATETM MODEL NO. B800
Radiology
47d
Cleared
Jun 05, 1985
RDIOGRAPHIC WALL HOLDER OR FILM RECEPTOR
Radiology
56d
Cleared
May 14, 1985
FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND
Radiology
116d
Cleared
Apr 09, 1985
XMA 325 (X-RAY GENERATOR)
Radiology
85d
Cleared
Apr 09, 1985
XMA INTEGRATED TABLE
Radiology
85d