# K990226: GE LOGIQ700 Diagnostic Ultrasound System with B-Flow

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, Inc.
- Decided: Feb 9, 1999 after 15 days
- Product code: IYO (System, Imaging, Pulsed Echo, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K930768 (1994). 2 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K930768: Orion Diagnostic Ultrasound System, GE Medical Systems (1994) Summary page 1.
- K960527: Logiq 1000 Diagnostic Ultrsound System, GE Medical Systems (1997) Summary page 1.

## Most influential descendants
- K993365: GE Logiq 700 with Harmonic Imaging Modification (1999), 0 descendants of its own
- K993364: GE Logiq 700 with Coded Excitation Modification (1999), 0 descendants of its own

## Indications for use
The LOGIQ 700 with B-flow is a general purpose ultrasound imaging system intended for use in the evaluation of soft tissue and vascular disease in the head, neck, chest, abdomen, pelvis, male and female reproductive organs, limbs and pregnant uterus.

Source page: https://510kreport.com/device/K990226
Methodology: https://510kreport.com/methodology