Mri Devices Corp. - FDA 510(k) Cleared Devices
71
Total
71
Cleared
0
Denied
Mri Devices Corp. has 71 FDA 510(k) cleared radiology devices. Based in Hartland, US.
Historical record: 71 cleared submissions from 1991 to 2004.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
71 devices
Cleared
Jul 21, 2004
DYNACAD V1.0
Radiology
69d
Cleared
Jul 19, 2004
MODEL BBC-127 BIOPSY BREAST COIL
Radiology
46d
Cleared
Mar 09, 2004
MODIFICATION TO HNC-127-INT NEUROVASCULAR ARRAY COIL
Radiology
26d
Cleared
Mar 09, 2004
MODIFICATION TO HRW-127 WRIST ARRAY COIL
Radiology
26d
Cleared
Mar 05, 2004
QSC-127-INT SHOULDER ARRAY COIL SET
Radiology
28d
Cleared
Jan 28, 2004
CLIPLOC SOFT TISSUE MARKER 18G/100MM (4), /130MM (5 1/8), /150MM (6), MODELS...
General & Plastic Surgery
91d
Cleared
Nov 25, 2003
MODELS HRK-63-8 PMS AND HRK-127-8 KNEE ARRAY COILS
Radiology
15d
Cleared
Oct 23, 2003
BIOPSY BREAST COIL, MODEL BBC
Radiology
64d
Cleared
Oct 10, 2003
KFA-12 KNEE, FOOT, AND ANKLE ARRAY COIL
Radiology
10d
Cleared
Oct 10, 2003
HAC-12 AND HAC-30 HEAD ARRAY COIL
Radiology
10d
Cleared
Sep 25, 2003
HRK-63-8 KNEE ARRAY COIL
Radiology
30d
Cleared
Aug 21, 2003
NEUROVASCULAR ARRAY COIL, MODEL NVA-127-8
Radiology
45d
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