# K902383: Steri-Cath (TM)

- Pathway: 510(k) (Traditional)
- Applicant: Concord/Portex
- Decided: Jul 12, 1990 after 43 days
- Product code: BSY (Catheters, Suction, Tracheobronchial)
- Device class: 1
- Regulation: 21 CFR 868.6810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K982239: Circuit Guard (1998), 0 descendants of its own
- K955645: Cath-Guide (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K902383
Methodology: https://510kreport.com/methodology