Sterling Diagnostic Imaging, Inc. is one of 20431 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sterling Diagnostic Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IIRAD DIRECTRAY OPERATOR CONSOLE, IISYS PACS SYSTEM, ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAIL
7
Total
7
Cleared
0
Denied
Sterling Diagnostic Imaging, Inc. has 7 FDA 510(k) cleared medical devices. Based in Newark, US.
Historical record: 7 cleared submissions from 1996 to 1998. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sterling Diagnostic Imaging, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sterling Diagnostic Imaging, Inc.
7 devices
Cleared
Jun 08, 1998
IIRAD DIRECTRAY OPERATOR CONSOLE
Radiology
84d
Cleared
Feb 13, 1998
IISYS PACS SYSTEM
Radiology
22d
Cleared
Dec 22, 1997
ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAIL
Radiology
28d
Cleared
Dec 04, 1997
STERLING DIAGNOSTIC IMAGING DIRECT RADIOGRAPHY
Radiology
100d
Cleared
Nov 10, 1997
RAVEN DRY PRINTER
Radiology
117d
Cleared
Oct 28, 1997
HELIOS LASER IMAGER 1417
Radiology
75d
Cleared
Dec 18, 1996
LINX NETWORKING SYSTEM
Radiology
55d