# K900805: Aloka 500 Diagnostic Ultrasound Scanning System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Information Technologies
- Decided: Aug 23, 1990 after 183 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.
4 later devices descend from it; 4 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K083254: Aloka Prousound 2 Diagnostic Ultrasound System (2008), 0 descendants of its own
- K070195: Broadsound, AL3C34A,AL7L50A, AL3C79B,AL7L24B, AT3P42A, AT3C52B, ATL5L40B, AT3P32A, AT3C42B (2007), 0 descendants of its own
- K990198: AMIB7 (1999), 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/K900805
Methodology: https://510kreport.com/methodology