# K954479: Dicomview

- Pathway: 510(k) (Traditional)
- Applicant: Heartlab, Inc.
- Decided: Feb 21, 1996 after 148 days
- Product code: LMD (System, Digital Image Communications, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
144 later devices descend from it; 1 cites it directly.
0 of 145 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K972229: Imageview Coronary Angiography Display and Review System (1997), 143 descendants of its own
- K994210: Inturis Suite (2000), 142 descendants of its own
- K022788: Philips Harmony Release 1 (2002), 129 descendants of its own
- K061995: Xcelera (2006), 128 descendants of its own
- K083348: Image-Arena Applications (2008), 89 descendants of its own

Source page: https://510kreport.com/device/K954479
Methodology: https://510kreport.com/methodology