Resonex, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Resonex, Inc. has 21 FDA 510(k) cleared radiology devices. Based in Sunnyvale, US.
Historical record: 21 cleared submissions from 1988 to 1994.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
21 devices
Cleared
Mar 21, 1994
FAST SPIN ECHO (FSE)
Radiology
137d
Cleared
Mar 16, 1994
NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEM
Radiology
118d
Cleared
Nov 02, 1993
ECG GATING UNIT
Radiology
228d
Cleared
Jan 12, 1993
3DTOF MRA
Radiology
162d
Cleared
Nov 23, 1992
KINEMATIC MRI MOVIEMAKER
Radiology
97d
Cleared
Oct 30, 1992
3D IMAGING
Radiology
92d
Cleared
Sep 04, 1992
MAGNETIZATION TRANSFER CONTRAST
Radiology
92d
Cleared
Jun 22, 1992
COILS FOR RX4000 & RX5000 MRI SYSTEMS
Radiology
153d
Cleared
May 28, 1992
BO POWER SUPPLY
Radiology
85d
Cleared
May 22, 1992
PRESATURATION
Radiology
88d
Cleared
Mar 16, 1992
16 BIT A/D
Radiology
84d
Cleared
Dec 04, 1991
2DTOF MAGNETIC RESONANCE ANGIOGRAPH (MRA)
Radiology
82d
Cleared
Nov 01, 1991
40-140 SPIN ECHO FLOW COMPENSATED PULSE SEQUENCE
Radiology
99d
Cleared
Jul 03, 1991
COIL FIELD EXTENDER
Radiology
71d
Cleared
Jun 20, 1991
RX-5000 MRI SYSTEM
Radiology
55d
Cleared
Apr 08, 1991
10 ADJUSTABLE BELT COIL
Radiology
76d
Cleared
Jul 19, 1990
BILATERAL TMJ COIL
Radiology
35d
Cleared
May 07, 1990
VERSION 4.3 APPLICATION SOFTWARE FOR USE W/RX-4000
Radiology
31d
Cleared
Sep 12, 1989
MOBILE RX-4000 MAGNETIC RESONANCE IMAGING SYSTEM
Radiology
36d
Cleared
Jun 01, 1989
VERSION 4.2 APPLICATION SOFTWARE
Radiology
38d
Cleared
Oct 13, 1988
VFQ HEAD COIL
Radiology
42d