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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