# K973070: Conveen Easicath Set

- Pathway: 510(k) (Traditional)
- Applicant: Coloplast Corp.
- Decided: Nov 6, 1997 after 80 days
- Product code: EZD (Catheter, Straight)
- Device class: 2
- Regulation: 21 CFR 876.5130
- 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 K910022 (1991). 1 ancestor in all.
55 later devices descend from it; 3 cite it directly.
0 of 57 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K910022: MMG/O'neil Urinary Catheterization System Kit, Medical Marketing Group (1991) Summary page 1.

## Most influential descendants
- K023254: Speedicath (2003), 53 descendants of its own
- K090960: Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184, (2009), 15 descendants of its own
- K110862: Vapro Plus Intermittent Catheter (2011), 14 descendants of its own
- K141642: Vapro Intermittent Catheter (2014), 13 descendants of its own
- K072808: Speedicath Compact (2007), 12 descendants of its own

## Indications for use
The Conveen® EasiCath Set is indicated for use by patients for intermittent catheterization for the purpose of bladder drainage.

Source page: https://510kreport.com/device/K973070
Methodology: https://510kreport.com/methodology