# K930200: Multi Dopplex II / Fetal Dopplex II

- Pathway: 510(k) (Traditional)
- Applicant: Huntleigh Healthcare, Inc.
- Decided: Jun 24, 1994 after 526 days
- Product code: KNG (Monitor, Ultrasonic, Fetal)
- Device class: 2
- Regulation: 21 CFR 884.2660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
52 later devices descend from it; 5 cite it directly.
0 of 53 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
- K991441: Cadence Doppler Ultrasound System (1999), 44 descendants of its own
- K024197: Lifedop Doppler (2003), 31 descendants of its own
- K040480: Sonotrax Ultrasonic Pocket Doppler (2004), 21 descendants of its own
- K080087: Sonotrax Ultrasonic Fetal and Vascular Pocket Doppler, Models Lite, Basic, Pro, II, II Pro and Vascular (2008), 13 descendants of its own
- K082480: Contec Pocket Fetal  Doppler (2009), 12 descendants of its own

Source page: https://510kreport.com/device/K930200
Methodology: https://510kreport.com/methodology