| 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 are the result-sets that are created
in response to DICOM Query/Retrieve requests that may be processed
| |
through Remote Procedure Calls.
Each entry in this table is one such result-set.
Result-sets are kept in this table, so that client-stations can
call Remote Procedures to obtain the content of a result-set in
portions of a limited size.
Also, since the creation of a result-set may need more time than
is reasonable wait for in a single Remote Procedure Call, the
| Property of the US Government. |
existence of this table makes it possible to call a first
Remote Procedure to create the result-set through a TaskMan process
and then call subsequent Remote Procedures to inquire whether
the result-set is complete, and subsequently to obtain the results.
| 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. |
| |
|
