# K924079: CFM-800 Color Flow Mapping System

- Pathway: 510(k) (Traditional)
- Applicant: Diasonics, Inc.
- Decided: Sep 28, 1993 after 411 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; 3 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
- K972973: Perception Inc. GPS-Tuv Diagnostic Ultrasound System (1997), 2 descendants of its own
- K981834: Perception Inc, GPS-6TBMD Diagnostic Ultrasound System (1998), 0 descendants of its own
- K974880: Perception GPS-RST Diagnostic Ultrasound System (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K924079
Methodology: https://510kreport.com/methodology