| 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 DICOM RETRIEVE REQUEST QUEUE is located on the DICOM Gateway.
| |
This file holds retrieve requests that are generated by VistA and DICOM Gateway to be
handled by a Retrieve Client Process on the DICOM Gateway.
The DICOM Gateway Retrieve Client Process uses the MAG DICOM Q/R CLIENT to pass
retrieve status information back to the VistA Q/R client.
This file should be truncated periodically, as there is no need for the
information in this file after the retrieve request has been processed.
| 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. |
| |
|
