# K863700: RT2800(115V)/H4008C and RT2800(220/240V)/H4008CE

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Feb 10, 1987 after 140 days
- Product code: ITX (Transducer, Ultrasonic, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 892.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
672 later devices descend from it; 2 cite it directly.
2 of 673 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
- K953752: RT55 Diagnostic Ultrasound System (1996), 669 descendants of its own
- K012560: GE Logiq A100 MP, Model 2272413 (2001), 668 descendants of its own
- K014206: Logiqbook (2002), 667 descendants of its own
- K032477: GE Logiq Book (2003), 666 descendants of its own
- K050126: GE Logiq Twin (2005), 665 descendants of its own

Source page: https://510kreport.com/device/K863700
Methodology: https://510kreport.com/methodology