FDA 510(k) Applications Submitted by STANDARD IMAGING, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K060532 |
02/28/2006 |
HDR 1000 PLUS WELL CHAMBER, MODEL 90008 |
STANDARD IMAGING, INC. |
K001825 |
06/16/2000 |
STANDARD IMAGING HDR 1000 PLUS ION CHAMBER; STANDARD IMAGING IVB 1000 ION CHAMBER |
STANDARD IMAGING, INC. |
K002833 |
09/12/2000 |
MODIFICATION TO STANDARD IMAGING PT 1000 ION CHAMBER |
STANDARD IMAGING, INC. |
K082773 |
09/22/2008 |
STANDARD IMAGING IMSURE BRACHY QA SOFTWARE, MODEL 91331 |
STANDARD IMAGING, INC. |
K042733 |
10/01/2004 |
STANDARD IMAGING PIPSPRO QA SOFTWARE SYSTEM |
STANDARD IMAGING, INC. |
K013548 |
10/24/2001 |
STANDARD IMAGING IVB 1000 WELL CHAMBER |
STANDARD IMAGING, INC. |
K040688 |
03/16/2004 |
STANDARD IMAGING E.IMRT CALCULATOR |
STANDARD IMAGING, INC. |
K103193 |
10/29/2010 |
DOSEVIEW 3D |
STANDARD IMAGING, INC. |
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