# K932106: Mobilett Plus Mobile X-Ray System

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Sep 14, 1994 after 499 days
- Product code: IZL (System, X-Ray, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K033238: Mobilette XP and Mobilett Xphybrid (2003), 4 descendants of its own
- K111912: Mobilett Mira (2011), 3 descendants of its own
- K193277: SOMATOM On.site and On.scene (2020), 1 descendant of its own
- K241295: SOMATOM On.site (2024), 0 descendants of its own
- K182639: MOBILETT Elara Max (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K932106
Methodology: https://510kreport.com/methodology