# K950279: TOMTECP90

- Pathway: 510(k) (Traditional)
- Applicant: Tomtec Imaging Systems, Inc.
- Decided: Sep 15, 1995 after 234 days
- Product code: LMB (Device, Digital Image Storage, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
26 later devices descend from it; 4 cite it directly.
0 of 27 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
- K964803: Univision Echocardiology System (1997), 24 descendants of its own
- K980060: Echolink (1998), 23 descendants of its own
- K023772: Kinetdx Picture Archiving and Communications System (2002), 16 descendants of its own
- K992259: Echocardiography System Series 95000 (1999), 16 descendants of its own
- K041029: Kinetdx (2004), 13 descendants of its own

Source page: https://510kreport.com/device/K950279
Methodology: https://510kreport.com/methodology