Medical Advances, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Advances, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL, MODEL 415PH-64/42: PHASED ARRAY SHOULDER COIL, MODEL 235GE-64
57
Total
57
Cleared
0
Denied
Medical Advances, Inc. has 57 FDA 510(k) cleared radiology devices. Based in Milwaukee, US.
Historical record: 57 cleared submissions from 1989 to 2002.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Advances, Inc.
57 devices
Cleared
Dec 16, 2002
MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL
Radiology
90d
Cleared
Jun 13, 2002
MODEL 415PH-64/42: PHASED ARRAY SHOULDER COIL
Radiology
38d
Cleared
Aug 14, 2001
MODEL 235GE-64
Radiology
81d
Cleared
Apr 03, 2001
MODEL 455GE PHASED ARRAY WRIST COIL
Radiology
84d
Cleared
Dec 22, 2000
MODEL 342GE-64 HIGH RESOLUTION BRAIN COIL
Radiology
22d
Cleared
Dec 13, 2000
MODEL 205GE-64: PATHWAY MRI CAROTID ARRAY COIL
Radiology
64d
Cleared
Apr 11, 2000
MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES
Radiology
68d
Cleared
Aug 02, 1999
QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64
Radiology
74d
Cleared
Jul 06, 1999
QUADRATURE WRIST COIL, MODEL 445PH-64
Radiology
71d
Cleared
Jun 10, 1999
`INEAR WRIST COIL, MODEL 440GE-09
Radiology
70d
Cleared
Jun 08, 1999
LINEAR SHOULDER COIL, MODEL 414GE-09
Radiology
68d
Cleared
Nov 23, 1998
MODEL 340GE-21C QUADRATURE BRAIN COIL
Radiology
90d
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