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FDA 510(k) Applications Submitted by TOM SCHUBERT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050299
02/07/2005
HRK-123 KNEE ARRAY COIL
MRI DEVICES CORPORATION
K020606
02/25/2002
NVA-63-8 NEUROVASCULAR ARRAY COIL
MRI DEVICES CORP.
K001713
06/05/2000
HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA
MRI DEVICES CORP.
K001944
06/26/2000
HAC-300 HEAD ARRAY COIL
MRI DEVICES CORP.
K032090
07/07/2003
NEUROVASCULAR ARRAY COIL, MODEL NVA-127-8
MRI DEVICES CORP.
K022372
07/22/2002
HRH-127-8 HEAD ARRAY COIL
MRI DEVICES CORP.
K042103
08/04/2004
NVA-63-8-A AND NVA-63-16-A NEUROVASCULAR ARRAY COIL
MRI DEVICES CORPORATION
K022588
08/05/2002
HRW-63-INT WRIST ARRAY COIL
MRI DEVICES CORP.
K032576
08/20/2003
BIOPSY BREAST COIL, MODEL BBC
MRI DEVICES CORP.
K032633
08/26/2003
HRK-63-8 KNEE ARRAY COIL
MRI DEVICES CORP.
K022883
08/30/2002
HRK-63 KNEE ARRAY COIL
MRI DEVICES CORP.
K052497
09/12/2005
NEUROVASCULAR ARRAY COIL, MODEL NVA-127-16-A
INVIVO CORP.
K013099
09/17/2001
MODIFICATION TO: QWH-420 WRIST ARRAY COIL
MRI DEVICES CORP.
K013159
09/21/2001
HRH-63-8 HEAD ARRAY COIL
MRI DEVICES CORP.
K013322
10/05/2001
HAC-420 HEAD ARRAY COIL
MRI DEVICES CORP.
K003505
11/13/2000
KFA-127 KNEE, FOOT AND ANKLE ARRAY
MRI DEVICES CORP.
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