| DESCRIPTION |
+---------------------------------------------------------------+
| The Food and Drug Administration classifies this software as |
| a medical device. As such, it may not be changed in any way. |
| Modifications to this software may result in an adulterated |
| medical device under 21CFR820, the use of which is considered |
| to be a violation of US Federal Statutes. |
| |
+---------------------------------------------------------------+
The entries in this table describe images that could not be processed
because the DICOM Gateway had no information about the "modality"
| |
that generated the image.
"Modalities" are defined in table 2006.582 (MODALITY TYPE DICTIONARY),
which is populated from the text-file xx:\DICOM\DICT\MODALITY.DIC.
The "C" cross-reference on this table organizes the problem-images
by the identifying properties of the "modality": manufacturer,
model, and modality-type.
| Property of the US Government. |
| No permission to copy or redistribute this software is given. |
| Use of unreleased versions of this software requires the user |
| to execute a written test agreement with the VistA Imaging |
| Development Office of the Department of Veterans Affairs, |
| telephone (301) 734-0100. |
| |
|
