# K010329: LOGIQ 500

- Pathway: 510(k) (Special)
- Applicant: General Electric Co.
- Decided: Mar 1, 2001 after 27 days
- Product code: IYN (System, Imaging, Pulsed Doppler, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1550
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
717 later devices descend from it; 6 cite it directly.
0 of 718 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
- K014097: GE Logiq 5 (2002), 657 descendants of its own
- K032974: GE Logiq 5 Pro or Expert (2003), 654 descendants of its own
- K060993: GE Logiq P5 and A5 (2006), 653 descendants of its own
- K032182: GE Logiq 7, Model 2354858 (2003), 631 descendants of its own
- K041813: GE Logiq 7 Ultrasound BT04 (2004), 630 descendants of its own

Source page: https://510kreport.com/device/K010329
Methodology: https://510kreport.com/methodology