Continental X-Ray Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Continental X-Ray Corp. - FDA 510(k) Cleared Devices
Recent clearances: CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002, ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300, CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105
27
Total
27
Cleared
0
Denied
Continental X-Ray Corp. has 27 FDA 510(k) cleared radiology devices. Based in Chicago, US.
Historical record: 27 cleared submissions from 1988 to 1997.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Continental X-Ray Corp.
27 devices
Cleared
Sep 11, 1997
CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002
Radiology
73d
Cleared
Jul 25, 1996
ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC...
Radiology
52d
Cleared
Jun 27, 1996
CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105
Radiology
57d
Cleared
Dec 21, 1995
ARC SERIES
Radiology
80d
Cleared
Mar 31, 1995
LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270
Radiology
59d
Cleared
Aug 17, 1994
LINEAR TOMOGRAPHIC SYSTEM: PMT 6000
Radiology
105d
Cleared
Jun 07, 1994
MODEL TM EP HIGH VOLTAGE GENERATOR
Radiology
42d
Cleared
May 26, 1994
MOLYBDENUM/RHODIUM FILTERS
Radiology
239d
Cleared
Jun 14, 1993
ELECTROPHYSIOLOGY (EP) TABLE EP 2000 SERIES
Radiology
82d
Cleared
Mar 04, 1993
WALL BUCKY HOLDERS LT. & RT. HAND, & CENTER MOUNT
Radiology
104d
Cleared
Oct 16, 1992
PATIENT INFORMATION MANAGER (PIM)
Radiology
171d
Cleared
Oct 15, 1992
X-RAY CONTROL AND HI-VOLTAGE GENERATOR
Radiology
178d