# K951925: Dicomit

- Pathway: 510(k) (Traditional)
- Applicant: Dicomit Imaging Systems Corp.
- Decided: Jul 12, 1995 after 78 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.
215 later devices descend from it; 2 cite it directly.
0 of 216 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
- K990248: Dicom Image Manager, Model 3-D Visualization Option (1999), 213 descendants of its own
- K992886: Powerview Ultrasound Workstation, Uidm-400A (1999), 212 descendants of its own
- K013633: Ssa-770A, Aplio Ultrasound System (2001), 211 descendants of its own
- K022400: Ssa-700A, Aplio Diagnostic Ultrasound System (2002), 210 descendants of its own
- K032281: Ssa-770A - Version 4, Aplio Diagnostic Ultrasound System (2003), 209 descendants of its own

Source page: https://510kreport.com/device/K951925
Methodology: https://510kreport.com/methodology