# K083520: Intelepacs, Model Version 3.X.X

- Pathway: 510(k) (Traditional)
- Applicant: Intelerad Medical Systems Incorporated
- Decided: Jun 23, 2009 after 209 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K150707: IntelePACS (2015), 2 descendants of its own
- K192176: IntelePACS (2020), 0 descendants of its own
- K162141: Restore PACS (2016), 0 descendants of its own

## Recalls of this device
- Jul 3, 2014 · Class II · Z-2267-2014: In specific situation a partially truncated file may be written to the IntelePACS server. This partially truncated file still can be viewed by InteleViewer and InteleViewer will report to the user tha

Source page: https://510kreport.com/device/K083520
Methodology: https://510kreport.com/methodology