# K011015: Catheter Repair Kit with Replacement Connector, Model 5587000

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Jun 22, 2001 after 79 days
- Product code: NFK (Kit, Repair, Catheter, Hemodialysis)
- 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.
8 later devices descend from it; 3 cite it directly.
0 of 9 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
- K022561: Catheter Repair Kit with Replacement Connector, Model 5587000 (2002), 4 descendants of its own
- K030442: Catheter Repair Kit with Replacement Connector, Model 5587000 (2003), 3 descendants of its own
- K063446: Catheter Repair Kit with Replacement Connector, Model 5587000 (2006), 2 descendants of its own
- K022644: Retro Repair Kit, Model PRRK5 (2002), 1 descendant of its own
- K101261: Catheter Repair Kit with Replacement Connector, Model 5587000 (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K011015
Methodology: https://510kreport.com/methodology