Usa Instruments, Inc. - FDA 510(k) Cleared Devices
64
Total
64
Cleared
0
Denied
Usa Instruments, Inc. has 64 FDA 510(k) cleared radiology devices. Based in Aurora, US.
Historical record: 64 cleared submissions from 1997 to 2005.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
64 devices
Cleared
Nov 09, 2005
USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY
Radiology
23d
Cleared
Oct 07, 2005
1.5T 12 CHANNEL BODY ARRAY
Radiology
17d
Cleared
Oct 07, 2005
1.5T 16 CHANNEL BRAIN-SPINE ARRAY COIL
Radiology
14d
Cleared
Oct 04, 2005
3T HD BREAST ARRAY
Radiology
14d
Cleared
Jun 28, 2005
OPEN BREAST COIL (OBC) WITH BIOPSY PLATES
Radiology
99d
Cleared
Sep 24, 2004
MILLENNIUM III 3T-8-CHANNEL NEUROVASCULAR COIL
Radiology
25d
Cleared
Aug 26, 2004
3.0T 8-CHANNEL CTL SPINE ARRAY
Radiology
14d
Cleared
Aug 26, 2004
11000 RAPTURE PHASED ARRAY PERIPHERAL VASCULAR COIL
Radiology
10d
Cleared
Aug 11, 2004
MARK III PHASED ARRAY SHOULDER COIL
Radiology
16d
Cleared
Jul 23, 2004
LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE
Radiology
31d
Cleared
Jun 17, 2004
QD HEAD SPEEDER WITH SPEEDER NV ATTACHMENT
Radiology
13d
Cleared
Jan 09, 2004
SPIRIT 5000 CARDIAC COIL
Radiology
66d
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