# K930090: Helicat

- Pathway: 510(k) (Traditional)
- Applicant: Elscint, Inc.
- Decided: Mar 19, 1993 after 70 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
267 later devices descend from it; 2 cite it directly.
0 of 268 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
- K961464: Select/SP (1996), 265 descendants of its own
- K982060: Volumax CT Imaging System (1998), 264 descendants of its own
- K012009: MX8000 Idt CT System (2001), 263 descendants of its own
- K033326: Philips Plus Computed Tomography System (2003), 214 descendants of its own
- K042293: Brilliance CT, Private Practice CV Configuration, CT Scanner (2004), 147 descendants of its own

Source page: https://510kreport.com/device/K930090
Methodology: https://510kreport.com/methodology