510(k) · Cleared
ClearedVapro Plus Intermittent Catheter
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Hollister Incorporated · GBM Catheter, Urethral
Cleared on Apr 26, 2011 as substantially equivalent to K090960 (Hollister, Inc., 2009) and 1 other predicate after a 28-day review. Its family tree reaches back 4 generations to 1991. 14 later devices descend from it.
- Decided
- Apr 26, 2011
- Review
- 28 days
- Class
- Class II
- Product code
- GBM
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 4 generations to K910022 (1991). 12 ancestors in all, the oldest K896750 (1990). 14 later devices descend from it, 1 citing it directly.
- Root · 4 generations backK910022 MMG/O'neil Urinary Catheterization System KitMedical Marketing Group · 1991
- 3 generations backK973070 Conveen Easicath SetColoplast Corp. · 1997
- 2 generations backK023254 SpeedicathColoplast Corp. · 2003
- 1 generation backK090960 Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142…Hollister, Inc. · 2009
- This deviceK110862 Vapro Plus Intermittent CatheterHollister Incorporated · 2011
- Descendant · cites it directly · 13 of its ownK141642 Vapro Intermittent CatheterHollister Incorporated · 2014
- Descendant · 2 generations on · 6 of its ownK180824 VaPro 2 Intermittent CatheterHollister Incorporated · 2018
- Descendant · 3 generations on · 3 of its ownK220667 Sleeved ICHollister Incorporated · 2022
- Descendant · 2 generations on · 3 of its ownK163179 Onli Intermittent CatheterHollister Incorporated · 2017
- Descendant · 4 generations on · 2 of its ownK233524 Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved…Hollister Incorporated · 2024
Showing 5 of 14 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 14 · See all- K141642Vapro Intermittent CatheterHollister Incorporated · 2014 · cites it directly13descendants
- K180824VaPro 2 Intermittent CatheterHollister Incorporated · 2018 · 2 generations on6descendants
- K220667Sleeved ICHollister Incorporated · 2022 · 3 generations on3descendants
- K163179Onli Intermittent CatheterHollister Incorporated · 2017 · 2 generations on3descendants
- K233524Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus (Name not…Hollister Incorporated · 2024 · 4 generations on2descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K910022 | MMG/O'neil Urinary Catheterization System Kit | Medical Marketing Group | 1991 | — |
| −3 | K973070 | Conveen Easicath Set | Coloplast Corp. | 1997 | — |
| −2 | K023254 | Speedicath | Coloplast Corp. | 2003 | — |
| −1 | K090960 | Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064… | Hollister, Inc. | 2009 | — |
| 0 (this device) | K110862 | Vapro Plus Intermittent Catheter | Hollister Incorporated | 2011 | — |
| +1 | K141642 | Vapro Intermittent Catheter | Hollister Incorporated | 2014 | — |
| +2 | K180824 | VaPro 2 Intermittent Catheter | Hollister Incorporated | 2018 | — |
| +3 | K220667 | Sleeved IC | Hollister Incorporated | 2022 | — |
| +2 | K163179 | Onli Intermittent Catheter | Hollister Incorporated | 2017 | — |
| +4 | K233524 | Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus… | Hollister Incorporated | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1990 | 1 | 0 |
| 1998 | 1 | 0 |
| 2001 | 4 | 0 |
| 2002 | 1 | 0 |
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2015 | 2 | 0 |
| 2017 | 1 | 0 |
| 2018 | 2 | 0 |
| 2019 | 2 | 0 |
| 2022 | 3 | 0 |
| 2024 | 1 | 0 |
| 2025 | 1 | 0 |
| 2026 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in GBM? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new GBM device
- #1 K241734 Wellead® Hydrophilic Intermittent Catheter…score 10.2 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K090960 | Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064, 72084…Summary page 1…the following products: Product 510(k) IVaProTM'Intermnittent Catheter IK090960 Incare Advance/Advance Plus K013483 Intermittent Catheter Device De… | 2009 |
| * | K013483 | Incare Advance; Intermittent Catheter, Plus Intermittent Catheter, Plus KitSummary page 1…uct 510(k) IVaProTM'Intermnittent Catheter IK090960 Incare Advance/Advance Plus K013483 Intermittent Catheter Device Description: The VaPro Plus intermittent catheter is a hydrophilic c… | 2002 |
What descends from it? (14)
See all 141 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K141642 | Vapro Intermittent Catheter | 2014 | 13 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 20 years and passes through 4 companies; a new generation was cleared every 6.6 years on median.
- 1 of the 12 ancestors has a recall of any class.
- Of its descendants, K141642 (Hollister Incorporated, 2014) has gone furthest, with 13 descendants of its own.
- 1 other device also cites its predicate K090960.
How does its category compare?
All GBM devicesGBM Catheter, Urethral: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · GBM
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GBM
230in 2020
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GBM
1in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · GBM
311in 2025
MAUDE reports naming product code GBM, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 2 | — | 0 | 5 |
| 2008 | 0 | — | 5 | 18 |
| 2009 | 1 | — | 0 | 3 |
| 2010 | 0 | — | 0 | 33 |
| 2011 | 2 | — | 1 | 46 |
| 2012 | 3 | 139 | 0 | 32 |
| 2013 | 0 | — | 0 | 41 |
| 2014 | 1 | — | 0 | 19 |
| 2015 | 5 | 76 | 0 | 21 |
| 2016 | 3 | 112 | 0 | 49 |
| 2017 | 2 | — | 0 | 59 |
| 2018 | 6 | 93 | 0 | 82 |
| 2019 | 7 | 121 | 0 | 148 |
| 2020 | 6 | 230 | 0 | 144 |
| 2021 | 0 | — | 0 | 102 |
| 2022 | 2 | — | 0 | 283 |
| 2023 | 0 | — | 1 (1) | 202 |
| 2024 | 0 | — | 0 | 468 |
| 2025 | 1 | — | 1 | 311 |
| 2026 | 0 | — | 1 | — |
What is it indicated for?
The VaPro Plus 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.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110862 · printed Nov 6, 2026
Cite this page
510(k) Report. “K110862: Vapro Plus Intermittent Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110862
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026