Xre Corp. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Xre Corp. has 20 FDA 510(k) cleared radiology devices. Based in Walker, US.
Historical record: 20 cleared submissions from 1977 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.
20 devices
Cleared
Dec 29, 1997
UNICATH SP BI-PLANE (MODEL M269 & M289)
Radiology
89d
Cleared
Jun 17, 1996
FULL FRAME ZOOM SYSTEM
Radiology
88d
Cleared
Apr 03, 1996
XRE COLLIMATOR
Radiology
22d
Cleared
Feb 27, 1995
UNICATH LLU ANGIOGRAPHIC SYSTEM
Radiology
112d
Cleared
Sep 09, 1994
CINEMAC QAS
Radiology
268d
Cleared
Apr 07, 1994
DVFX, MODEL M256
Radiology
265d
Cleared
Dec 17, 1992
BI-N
Radiology
80d
Cleared
Nov 20, 1992
POLY DIAGNOST CDX
Radiology
122d
Cleared
Nov 07, 1991
UNICATH EP.
Radiology
80d
Cleared
Aug 28, 1991
ANGIOGRAPHIC OR FLUOROSCOPIC X-RAY SYSTEM
Radiology
89d
Cleared
Aug 09, 1989
UNICATH A
Radiology
113d
Cleared
Jan 29, 1988
UNICATH LAB
Radiology
38d
Cleared
Nov 16, 1987
OMNI DIAGNOST
Radiology
38d
Cleared
Nov 16, 1987
TRAUMA TABLE II
Radiology
38d
Cleared
Oct 28, 1985
OMNI PLANE SYSTEM
Radiology
21d
Cleared
Sep 26, 1985
TRAUMA STAND
Radiology
77d
Cleared
Sep 11, 1985
TRAUMA TABLE
General & Plastic Surgery
19d
Cleared
May 06, 1985
QUANTIX CARDIAC ANGIOGRAPHIC SYSTEM
Radiology
89d
Cleared
Jun 28, 1983
DENTAL CASSETTE HOLDERS
Radiology
63d
Cleared
Jan 05, 1977
RADIAL TRAVEL SPEC. PROCEDURES TABLE
Radiology
9d