| 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. |
| |
+---------------------------------------------------------------+
This file contains information about studies
for which all images have been transmitted
| |
to a VistA DICOM Gateway.
When all images for a study have been transmitted,
the study (or examination, or briefly, 'exam')
is called 'complete'.
The information that is collected for each study
consists of a flag that indicated whether or
not the exam is complete,
an accession number,
| Property of the US Government. |
a patient ID as well as the patient's name,
and an unique identifier for the study (UID).
| 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. |
| |
|
