# K920374: Aloka 650CL Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Information Technologies
- Decided: Apr 2, 1992 after 64 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
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K972192: Perception Inc. GPS-Xyz Diagnostic Ultrasound System (1997), 1 descendant of its own
- K981834: Perception Inc, GPS-6TBMD Diagnostic Ultrasound System (1998), 0 descendants of its own
- K974301: CLK Int'l. Sanitary Latex Probe Cover, CLK Ultrasound Probe Cover (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K920374
Methodology: https://510kreport.com/methodology