| 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 Imaging Site Parameter file contains those variables which are site
specific, and which are necessary for the Imaging Software to perform
| |
properly. Most of the fields have MUMPs cross-references with which they
are associated that are used by the software for quick access to the
specific data. Some of the fields defined may not be in use presently, but
are reserved for future development. Review the Imaging Installation
Manual for instructions on making entries into this file.
Non-integrated sites and Integrated sites that have one shared image
storage location have one record. Integrated sites where each site has
their own image storage have one record for each of the associated sites.
| 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. |
| |
|
