# K180824: VaPro 2 Intermittent Catheter

- Pathway: 510(k) (Special)
- Applicant: Hollister Incorporated
- Decided: Jun 22, 2018 after 84 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: 6 generations back to K910022 (1991). 14 ancestors in all.
6 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141642: Vapro Intermittent Catheter, Hollister Incorporated (2014) Summary page 4.

## Most influential descendants
- K220667: Sleeved IC (2022), 3 descendants of its own
- K233524: Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus (Name not Finalized); Sleeved IC 2 Pocket (Name not Finalized); Sleeved IC 2 Plus Pocket (Name not Finalized) (2024), 2 descendants of its own
- K183253: ValPro 2 Plus, VaPro 2 Plus Pocket (2018), 1 descendant of its own
- K253295: Coude Sleeved IC; Coude Plus Sleeved IC (2026), 0 descendants of its own
- K251468: Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket (name not finalized) Sleeved IC 3 Plus (name not finalized) Sleeved IC 3 Plus Pocket (name not finalized) (N/A) (2025), 0 descendants of its own

## Indications for use
This 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/K180824
Methodology: https://510kreport.com/methodology