Medicor USA , Ltd. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Medicor USA , Ltd. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1978 to 1986. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Medicor USA , Ltd. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Jul 18, 1986
MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEM
Radiology
56d
Cleared
Jun 19, 1986
MODEL RS-3 RADIOGRAPHIC STAND
Radiology
27d
Cleared
May 07, 1986
MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR
Radiology
124d
Cleared
Sep 19, 1985
MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C
Radiology
206d
Cleared
Jul 01, 1985
MODEL BION 2/TYPE 90 ROOM IONIZER
General Hospital
88d
Cleared
Jun 19, 1985
MODEL BION 1/TYPE 1084T CAR IONIZER
General Hospital
92d
Cleared
Nov 27, 1984
FLOOR MOUNTED X-RAY TUBESTAND
Radiology
92d
Cleared
Mar 23, 1984
UROLIX-3 UROLOGICAL TABLE
Radiology
64d
Cleared
Mar 22, 1984
C-ARM CEILING CRANE FT-2
Radiology
63d
Cleared
Mar 16, 1984
MOTOR TILTED EXAM. TABLE UV-56
Radiology
57d
Cleared
Jan 14, 1983
CPM METABOLIC MONITOR
Anesthesiology
37d
Cleared
Aug 16, 1979
MEDICOR QUALITY CONTROL BUFFER
Chemistry
37d