510(k) Report

510(k) · Cleared

Cleared

VaPro 2 Intermittent Catheter

K180824510(k) SpecialCleared Jun 22, 201884-day reviewClass II21 CFR 876.5130

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Hollister Incorporated · GBM Catheter, Urethral

Cleared on Jun 22, 2018 as substantially equivalent to K141642 (Hollister Incorporated, 2014) after an 84-day review. Its family tree reaches back 6 generations to 1991. 6 later devices descend from it.

Decided
Jun 22, 2018
Review
84 days
Class
Class II
Product code
GBM
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K910022 (1991). 14 ancestors in all, the oldest K896750 (1990). 6 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2002: 1 other ancestor2001: 4 other ancestors1998: 1 other ancestor1990: 1 other ancestor2022: 1 descendant cleared2018: 1 descendant cleared2019: 1 descendant cleared2024: 1 descendant cleared2025: 1 descendant cleared2026: 1 descendant clearedReference device: K143594 · VaPro Pocket · Hollister Incorporated · 2015K910022 · MMG/O'neil Urinary Catheterization System Kit · Medical Marketing Group · 1991K973070 · Conveen Easicath Set · Coloplast Corp. · 1997K023254 · Speedicath · Coloplast Corp. · 2003K090960 · Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184, · Hollister, Inc. · 2009K110862 · Vapro Plus Intermittent Catheter · Hollister Incorporated · 2011K141642 · Vapro Intermittent Catheter · Hollister Incorporated · 20141990200020102020
  1. Root · 6 generations backK910022 MMG/O'neil Urinary Catheterization System KitMedical Marketing Group · 1991
  2. 5 generations backK973070 Conveen Easicath SetColoplast Corp. · 1997
  3. 4 generations backK023254 SpeedicathColoplast Corp. · 2003
  4. 3 generations backK090960 Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142…Hollister, Inc. · 2009
  5. 2 generations backK110862 Vapro Plus Intermittent CatheterHollister Incorporated · 2011
  6. 1 generation backK141642 Vapro Intermittent CatheterHollister Incorporated · 2014
  7. This deviceK180824 VaPro 2 Intermittent CatheterHollister Incorporated · 2018
  8. Descendant · cites it directly · 3 of its ownK220667 Sleeved ICHollister Incorporated · 2022
  9. Descendant · 2 generations on · 2 of its ownK233524 Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved…Hollister Incorporated · 2024
  10. Descendant · cites it directly · 1 of its ownK183253 ValPro 2 Plus, VaPro 2 Plus PocketHollister Incorporated · 2018
  11. Descendant · 3 generations on · 0 of its ownK253295 Coude Sleeved IC; Coude Plus Sleeved ICHollister Incorporated · 2026
  12. Descendant · 3 generations on · 0 of its ownK251468 Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC…Hollister Incorporated · 2025

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2018: 12019: 12022: 12024: 12025: 12026: 1
2018high 1 (2018) · low 0 (2020)2026

Most influential descendants

Showing 5 of 6 · See all
  • K220667Sleeved ICHollister Incorporated · 2022 · cites it directly3descendants
  • K233524Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus (Name not…Hollister Incorporated · 2024 · 2 generations on2descendants
  • K183253ValPro 2 Plus, VaPro 2 Plus PocketHollister Incorporated · 2018 · cites it directly1descendant
  • K253295Coude Sleeved IC; Coude Plus Sleeved ICHollister Incorporated · 2026 · 3 generations on0descendants
  • K251468Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket (name not…Hollister Incorporated · 2025 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K910022MMG/O'neil Urinary Catheterization System KitMedical Marketing Group1991—
−5K973070Conveen Easicath SetColoplast Corp.1997—
−4K023254SpeedicathColoplast Corp.2003—
−3K090960Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064…Hollister, Inc.2009—
−2K110862Vapro Plus Intermittent CatheterHollister Incorporated2011—
−1K141642Vapro Intermittent CatheterHollister Incorporated2014—
0 (this device)K180824VaPro 2 Intermittent CatheterHollister Incorporated2018—
+1K220667Sleeved ICHollister Incorporated2022—
+2K233524Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus…Hollister Incorporated2024—
+1K183253ValPro 2 Plus, VaPro 2 Plus PocketHollister Incorporated2018—
+3K253295Coude Sleeved IC; Coude Plus Sleeved ICHollister Incorporated2026—
+3K251468Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket…Hollister Incorporated2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199810
200140
200210
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201810
201910
202210
202410
202510
202610
FIG. 1 — Lineage of K180824, 1991–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K241734 Wellead® Hydrophilic Intermittent Catheter…score 10.2 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K141642Vapro Intermittent Catheter
Summary page 4
…21 CRF 876.5130 Predicate Device: VaPro 2 Intermittent Catheter is substantially equivalent to its original design: VaPro Intermittent Catheter, K141642 by Hollister Incorporated Reference Device: VaPro Pocket, K143594 by Hollister Incorporated for VaPro 2 Pocket. Indications fo…
Hollister Incorporated2014—
†K143594VaPro PocketHollister Incorporated2015—

Also cleared against K141642: 3 other devices →

What descends from it? (6)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K220667Sleeved ICHollister Incorporated20223
K183253ValPro 2 Plus, VaPro 2 Plus PocketHollister Incorporated20181

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 27 years and passes through 4 companies; a new generation was cleared every 5.2 years on median.
  • 1 of the 14 ancestors has a recall of any class.
  • Of its descendants, K220667 (Hollister Incorporated, 2022) has gone furthest, with 3 descendants of its own.
  • 3 other devices also cite its predicate K141642.

How does its category compare?

All GBM devices

GBM Catheter, Urethral: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · GBM

1in 2025

2007: 22009: 12011: 22012: 32014: 12015: 52016: 32017: 22018: 62019: 72020: 62022: 22025: 1
2007high 7 (2019) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GBM

230in 2020

2012: 139 days median2015: 76 days median2016: 112 days median2018: 93 days median2019: 121 days median2020: 230 days median
2007high 230 (2020) · low 76 (2015)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GBM

1in 2025

2008: 52011: 12023: 1, 1 Class I2025: 12026 (partial year): 1
2007high 5 (2008) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GBM

311in 2025

2007: 52008: 182009: 32010: 332011: 462012: 322013: 412014: 192015: 212016: 492017: 592018: 822019: 1482020: 1442021: 1022022: 2832023: 2022024: 4682025: 311
2007high 468 (2024) · low 3 (2009)2025

MAUDE reports naming product code GBM, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—05
20080—518
20091—03
20100—033
20112—146
20123139032
20130—041
20141—019
2015576021
20163112049
20172—059
2018693082
201971210148
202062300144
20210—0102
20222—0283
20230—1 (1)202
20240—0468
20251—1311
20260—1—

What is it indicated for?

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.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K180824: VaPro 2 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/K180824

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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