# K023024: Transvaginal Doppler Probe, Model 09-0006-02

- Pathway: 510(k) (Traditional)
- Applicant: Vascular Control Systems, Inc.
- Decided: Sep 26, 2002 after 15 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
Longest line of descent: 1 generation back to K935994 (1995). 1 ancestor in all.
2 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)
- K935994: PW Doppler Vascular Probes, Koven Technology, Inc. (1995) Summary page 1.

## Most influential descendants
- K032125: Cstat, Models 09-0014-01 and 09-0014-02 (2004), 0 descendants of its own
- K031358: Transvaginal Doppler Probe (2003), 0 descendants of its own

## Indications for use
The Transvaginal Doppler Probe is intended for bilateral detection of uterine blood vessels.

Source page: https://510kreport.com/device/K023024
Methodology: https://510kreport.com/methodology