# K951144: Phoenix Plus & Base Nuclear Medicine Single Detector Systems

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Jul 3, 1995 after 112 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
17 later devices descend from it; 1 cites it directly.
1 of 18 devices in its family (counting itself) has 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
- K962738: Millennium MT and Millennium MG Nuclear Medicine Systems (1996), 16 descendants of its own
- K022240: Mobile Millennium MG System (2002), 11 descendants of its own
- K090811: Inspira HD, Model: NL1000 (2009), 10 descendants of its own
- K102677: Bodytom NL 4000 (2011), 9 descendants of its own
- K170238: BodyTom Elite (2017), 4 descendants of its own

Source page: https://510kreport.com/device/K951144
Methodology: https://510kreport.com/methodology