# K931393: Bebig Plaques RUM101-RUM114

- Pathway: 510(k) (Traditional)
- Applicant: Bebig, Inc.
- Decided: Mar 16, 1994 after 362 days
- Product code: KXK (Source, Brachytherapy, Radionuclide)
- Device class: 2
- Regulation: 21 CFR 892.5730
- 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; 1 cites 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
- K090321: Ric Conformal Source, Model 100 (2009), 2 descendants of its own
- K252296: OncoPatch (2025), 0 descendants of its own
- K191324: CivaDerm (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K931393
Methodology: https://510kreport.com/methodology