# K974570: Peritoneal Dialysis Catheter Connector

- Pathway: 510(k) (Traditional)
- Applicant: Medigroup, Inc.
- Decided: Feb 27, 1998 after 81 days
- Product code: FKO (Catheter, Peritoneal Dialysis, Single Use)
- Device class: 2
- Regulation: 21 CFR 876.5630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K910787 (1991). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K910787: Titanium Connector (2 Part), Accurate Surgical Instruments Co. (1991) Summary page 1.

## Indications for use
Peritoneal dialysis connectors are used to connect the peritoneal dialysis catheter to the dialysate line.

Source page: https://510kreport.com/device/K974570
Methodology: https://510kreport.com/methodology