Standard Imaging, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Standard Imaging, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Standard Imaging, Inc. has 10 FDA 510(k) cleared radiology devices. Based in Middleton, US.
Historical record: 10 cleared submissions from 1992 to 2010.
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 - Standard Imaging, Inc.
10 devices
Cleared
Dec 27, 2010
DOSEVIEW 3D
Radiology
59d
Cleared
Nov 19, 2008
STANDARD IMAGING IMSURE BRACHY QA SOFTWARE, MODEL 91331
Radiology
58d
Cleared
Apr 11, 2006
HDR 1000 PLUS WELL CHAMBER, MODEL 90008
Radiology
42d
Cleared
Nov 15, 2004
STANDARD IMAGING PIPSPRO QA SOFTWARE SYSTEM
Radiology
45d
Cleared
May 11, 2004
STANDARD IMAGING E.IMRT CALCULATOR
Radiology
56d
Cleared
Nov 09, 2001
STANDARD IMAGING IVB 1000 WELL CHAMBER
Radiology
16d
Cleared
Sep 28, 2000
MODIFICATION TO STANDARD IMAGING PT 1000 ION CHAMBER
Radiology
16d
Cleared
Aug 02, 2000
STANDARD IMAGING HDR 1000 PLUS ION CHAMBER
Radiology
47d
Cleared
Mar 16, 1994
STAND IMAGING DOSE CALIBRATOR SHIELDED WORK PLATFORM
Radiology
37d
Cleared
Aug 24, 1992
STANDARD IMAGING HDR 1000 ION CHAMBER
Radiology
87d