# K970969: Kendall Curity Suprapubic Catheter Tray, Kit, & Replacement Set

- Pathway: 510(k) (Traditional)
- Applicant: The Kendal Co.
- Decided: Apr 23, 1997 after 37 days
- Product code: KOB (Catheter, Suprapubic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5090
- 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 K842899 (1984). 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)
- K842899: Curity Suprapubic Drainage System, The Kendal Co. (1984) Summary page 1.

## Indications for use
The Kendall CURITY Suprapubic Catheter Trays and kits are intended to provide urinary bladder drainage or irrigation by percutaneous placement of a suprapubic catheter. This is a useful method of controlling urinary bladder drainage postoperatively.

Source page: https://510kreport.com/device/K970969
Methodology: https://510kreport.com/methodology