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
Cleared
Jun 28, 1979
SYRINGE TONOMETER
Chemistry
64d
Cleared
Sep 20, 1978
PRECISION GAS MIXER
Chemistry
35d