| 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. |
| |
+---------------------------------------------------------------+
Anatomic Pathology images are associated with TIU documents that
contain the diagnostic report. Until the TIU document is created,
| |
this Imaging file temporarily records the association for the
Anatomic Pathology image entries. The Lab package notifies Imaging
when an Anatomic Pathology case is electronically signed and a TIU
note is created for the report. Imaging then changes the association
parent data file to the TIU document(actually the TIU EXTERNAL DATA
LINK file (#8925.91)). The entry in this file is then deleted.
If the TUI document exists at the time that the image is acquired,
the association is made to it and this file is not used.
| 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. |
| |
|
