510(k) · Cleared
ClearedPharma-Plast Urinary Drainage Bag 2000
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Zimmar Consulting, Ltd. · KNX Collector, Urine, (And Accessories) For Indwelling Catheter
Cleared on Oct 11, 1984 after a 35-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.
- Decided
- Oct 11, 1984
- Review
- 35 days
- Class
- Class II
- Product code
- KNX
- Recalls
- None
- Predicates
- 0
1 later device descends from it, 1 citing it directly.
- This deviceK843480 Pharma-Plast Urinary Drainage Bag 2000Zimmar Consulting, Ltd. · 1984
- Descendant · cites it directly · 0 of its ownK973364 4L Drainage Bag, 4L Bag for Peritoneal Dialysis, 4L Urinary Drainage…Maersk Medical A/S · 1998
Most influential descendants
Showing 1 of 1 · See all- K9733644L Drainage Bag, 4L Bag for Peritoneal Dialysis, 4L Urinary Drainage BagMaersk Medical A/S · 1998 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K843480 | Pharma-Plast Urinary Drainage Bag 2000 | Zimmar Consulting, Ltd. | 1984 | — |
| +1 | K973364 | 4L Drainage Bag, 4L Bag for Peritoneal Dialysis, 4L Urinary Drainage Bag | Maersk Medical A/S | 1998 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 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 KNX? 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? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K973364 | 4L Drainage Bag, 4L Bag for Peritoneal Dialysis, 4L Urinary Drainage Bag | 1998 | 0 |
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, K973364 (Maersk Medical A/S, 1998) has gone furthest, with 0 descendants of its own.
How does its category compare?
All KNX devicesKNX Collector, Urine, (And Accessories) For Indwelling Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KNX
1in 2011
2026 to Oct 25, outlined.
Median 510(k) review, days · KNX
Too few KNX 510(k)s in any year since 2007 to give a median.
Recalls per year · KNX
1in 2023
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · KNX
196in 2025
MAUDE reports naming product code KNX, 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 | 1 |
| 2008 | 0 | — | 0 | 3 |
| 2009 | 0 | — | 0 | 4 |
| 2010 | 0 | — | 0 | 11 |
| 2011 | 1 | — | 3 | 7 |
| 2012 | 0 | — | 0 | 16 |
| 2013 | 0 | — | 0 | 4 |
| 2014 | 0 | — | 0 | 15 |
| 2015 | 0 | — | 0 | 21 |
| 2016 | 0 | — | 1 | 82 |
| 2017 | 0 | — | 0 | 154 |
| 2018 | 0 | — | 0 | 190 |
| 2019 | 0 | — | 0 | 235 |
| 2020 | 0 | — | 0 | 215 |
| 2021 | 0 | — | 0 | 209 |
| 2022 | 0 | — | 0 | 167 |
| 2023 | 0 | — | 1 (1) | 178 |
| 2024 | 0 | — | 0 | 162 |
| 2025 | 0 | — | 0 | 196 |
| 2026 | 0 | — | 2 | — |
https://510kreport.com/device/K843480 · printed Nov 4, 2026
Cite this page
510(k) Report. “K843480: Pharma-Plast Urinary Drainage Bag 2000.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K843480
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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