# K992208: GE Logiq 200 MD Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, Inc.
- Decided: Jul 12, 1999 after 12 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 K863700 (1987). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960700: Logiq  A200 Diagnostic Ultrasound System, GE Medical Systems (1996) Summary page 6.

## Indications for use
2D ultrasound imaging or motion analysis as follows:

Source page: https://510kreport.com/device/K992208
Methodology: https://510kreport.com/methodology