| 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 activities that are requested
by DICOM Gateways, to be performed by procedures that are
| |
executed remotely on a VistA Server.
The name of the Remote Procedure that processed these requests
is MAG DICOM IMAGE PROCESSING; the code for this procedure
starts at ENTRY^MAGDIR8.
The data in the various request-records contains a code that
speficies the type of operation, and any subsequent data
in the request are parameters for that operation.
| Property of the US Government. |
Currently, the following requests are recognized:
(upper case values are constants, lower case values
indicate variable values):
PROCESSED|0|location|instrument|image|1
CORRECT|PROCESSED|image|study|deletion|instrument|filename|study_uid|gateway_id
The data in this file is extremely volatile.
Records will be entered, processed and deleted in rapid progression.
| 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. |
| |
|
