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FDA 510(k) Applications Submitted by MRI DEVICES CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050514
03/01/2005
MODELS FAC-63 AND FAC-127 FOOT AND ANKLE COILS
MRI DEVICES CORPORATION
K050621
03/10/2005
NVA-127-8-A NEUROVASCULAR ARRAY COIL
MRI DEVICES CORPORATION
K050622
03/10/2005
HRW-63-8 WRIST ARRAY COIL; HRW-127-8 WRIST ARRAY COIL
MRI DEVICES CORPORATION
K050299
02/07/2005
HRK-123 KNEE ARRAY COIL
MRI DEVICES CORPORATION
K042103
08/04/2004
NVA-63-8-A AND NVA-63-16-A NEUROVASCULAR ARRAY COIL
MRI DEVICES CORPORATION
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