# K102905: Guided Medical Positioning System II (GMPS II)

- Pathway: 510(k) (Special)
- Applicant: Mediguide, Ltd.
- Decided: Oct 29, 2010 after 29 days
- Product code: DQK (Computer, Diagnostic, Programmable)
- Device class: 2
- Regulation: 21 CFR 870.1425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
43 later devices descend from it; 1 cites it directly.
5 of 44 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
- K120301: Mediguide Technology (2012), 42 descendants of its own
- K160210: EnSite Precision Cardiac Mapping System v2.0 (2016), 29 descendants of its own
- K172396: EnSite Velocity Cardiac Mapping System v5.2 (2018), 27 descendants of its own
- K182644: EnSite Velocity Cardiac Mapping System v5.2, EnSite Precision Cardiac Mapping System v2.2 (2018), 26 descendants of its own
- K183128: EnSite Velocity Cardiac Mapping System v5.2, EnSite Precision Cardiac Mapping System v2.2 (2018), 25 descendants of its own

Source page: https://510kreport.com/device/K102905
Methodology: https://510kreport.com/methodology