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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