# K090960: Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,

- Pathway: 510(k) (Traditional)
- Applicant: Hollister, Inc.
- Decided: Aug 20, 2009 after 136 days
- Product code: GBM (Catheter, Urethral)
- 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: 3 generations back to K910022 (1991). 11 ancestors in all.
15 later devices descend from it; 2 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050874: Astra Tech AB Lofric Primo Single Use Urinary Catheter, Astra Tech, Inc. (2005) Summary page 1.
- K023254: Speedicath, Coloplast Corp. (2003) Summary page 1.
- K013483: Incare Advance; Intermittent Catheter, Plus Intermittent Catheter, Plus Kit, Hollister, Inc. (2002) Summary page 1.

## Most influential descendants
- K110862: Vapro Plus Intermittent Catheter (2011), 14 descendants of its own
- K141642: Vapro Intermittent Catheter (2014), 13 descendants of its own
- K180824: VaPro 2 Intermittent Catheter (2018), 6 descendants of its own
- K220667: Sleeved IC (2022), 3 descendants of its own
- K163179: Onli Intermittent Catheter (2017), 3 descendants of its own

## Indications for use
The VaPro intermittent catheter is a flexible tubular device that is inserted through the urethra by male, female and pediatric patients who need to drain urine from the bladder.

Source page: https://510kreport.com/device/K090960
Methodology: https://510kreport.com/methodology