510(k) · Cleared
ClearedBard Hysterosalpingography Catheters
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
C.R. Bard, Inc. · HES Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)
Cleared on Apr 25, 1989 after a 63-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it.
- Decided
- Apr 25, 1989
- Review
- 63 days
- Class
- Class II
- Product code
- HES
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 1 citing it directly.
- This deviceK890869 Bard Hysterosalpingography CathetersC.R. Bard, Inc. · 1989
- Descendant · cites it directly · 3 of its ownK061679 Wallace Artificial Insemination CatheterIrvine Scientific Sales Co., Inc. · 2006
- Descendant · 2 generations on · 1 of its ownK131491 Kitazato Iui CatheterKitazato Medical Co., Ltd. · 2013
- Descendant · 2 generations on · 0 of its ownK163318 Soules Intrauterine Insemination CatheterCook Incorporated · 2017
- Descendant · 3 generations on · 0 of its ownK162667 Kitazato IUI CatheterKitazato Corporation · 2017
Most influential descendants
Showing 4 of 4 · See all- K061679Wallace Artificial Insemination CatheterIrvine Scientific Sales Co., Inc. · 2006 · cites it directly3descendants
- K131491Kitazato Iui CatheterKitazato Medical Co., Ltd. · 2013 · 2 generations on1descendant
- K163318Soules Intrauterine Insemination CatheterCook Incorporated · 2017 · 2 generations on0descendants
- K162667Kitazato IUI CatheterKitazato Corporation · 2017 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K890869 | Bard Hysterosalpingography Catheters | C.R. Bard, Inc. | 1989 | — |
| +1 | K061679 | Wallace Artificial Insemination Catheter | Irvine Scientific Sales Co., Inc. | 2006 | — |
| +2 | K131491 | Kitazato Iui Catheter | Kitazato Medical Co., Ltd. | 2013 | — |
| +2 | K163318 | Soules Intrauterine Insemination Catheter | Cook Incorporated | 2017 | — |
| +3 | K162667 | Kitazato IUI Catheter | Kitazato Corporation | 2017 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2013 | 1 | 0 |
| 2017 | 2 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in HES? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K061679 | Wallace Artificial Insemination Catheter | 2006 | 3 |
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?
- Of its descendants, K061679 (Irvine Scientific Sales Co., Inc., 2006) has gone furthest, with 3 descendants of its own.
How does its category compare?
All HES devicesHES Insufflator, Carbon-Dioxide, Uterotubal (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · HES
1in 2014
2026 to Oct 25, outlined.
Median 510(k) review, days · HES
Too few HES 510(k)s in any year since 2007 to give a median.
Recalls per year · HES
No recall names HES since 2007.
Adverse event reports per year · HES
1in 2025
MAUDE reports naming product code HES, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 2 |
| 2013 | 0 | — | 0 | 1 |
| 2014 | 1 | — | 0 | 2 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 5 |
| 2017 | 0 | — | 0 | 29 |
| 2018 | 0 | — | 0 | 68 |
| 2019 | 0 | — | 0 | 31 |
| 2020 | 0 | — | 0 | 16 |
| 2021 | 0 | — | 0 | 1 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 1 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K890869 · printed Nov 6, 2026
Cite this page
510(k) Report. “K890869: Bard Hysterosalpingography Catheters.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K890869
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026