# K010778: Niagara Slim-Cath

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: Apr 13, 2001 after 29 days
- Product code: MPB (Catheter, Hemodialysis, Non-Implanted)
- Device class: 2
- Regulation: 21 CFR 876.5540
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
18 later devices descend from it; 5 cite it directly.
5 of 19 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
- K083675: Power-Trialysis Triple Lumen Acute Dialysis Catheter (2009), 12 descendants of its own
- K102605: Mahurkar Triple Lumen Dialysis Catheter (2010), 7 descendants of its own
- K133456: Power-Trialysis Short-Term Dialysis Catheter (2014), 2 descendants of its own
- K123292: T3 (2013), 2 descendants of its own
- K183219: Trio-CT Triple Lumen Catheter (2019), 1 descendant of its own

Source page: https://510kreport.com/device/K010778
Methodology: https://510kreport.com/methodology