| 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 a number of parameters about image
files that have been received by a DICOM Image Gateway.
| |
Entries are placed into this table (automatically) when a C-Store processor
delivers a file to the Image Gateway.
Entries are removed from this table (automatically) when the "Process Images"
task on the Image Gateway processes the image in question.
| 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. |
| |
|
