510(k) · Cleared
ClearedMulti-AD Fluid Dispensing System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
National Patent Development Corp. · KYX Dispenser, Liquid Medication
Cleared on Dec 20, 1979 after a 45-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 3 later devices descend from it.
- Decided
- Dec 20, 1979
- Review
- 45 days
- Class
- Class I
- Product code
- KYX
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 3 citing it directly.
- This deviceK792227 Multi-AD Fluid Dispensing SystemNational Patent Development Corp. · 1979
- Descendant · cites it directly · 1 of its ownK063851 Auto-Fill Syringe Kit, Model 7600Vascular Solutions, Inc. · 2007
- Descendant · cites it directly · 0 of its ownK131661 Infusion Syringe SetInnovative Medical Manufacturing Co. · 2013
- Descendant · cites it directly · 0 of its ownK955398 Formulation Preparation DeviceB.Braun Medical, Inc. · 1996
Most influential descendants
Showing 3 of 3 · See all- K063851Auto-Fill Syringe Kit, Model 7600Vascular Solutions, Inc. · 2007 · cites it directly1descendant
- K131661Infusion Syringe SetInnovative Medical Manufacturing Co. · 2013 · cites it directly0descendants
- K955398Formulation Preparation DeviceB.Braun Medical, Inc. · 1996 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K792227 | Multi-AD Fluid Dispensing System | National Patent Development Corp. | 1979 | — |
| +1 | K063851 | Auto-Fill Syringe Kit, Model 7600 | Vascular Solutions, Inc. | 2007 | — |
| +1 | K131661 | Infusion Syringe Set | Innovative Medical Manufacturing Co. | 2013 | — |
| +1 | K955398 | Formulation Preparation Device | B.Braun Medical, Inc. | 1996 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 2007 | 1 | 0 |
| 2013 | 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 KYX? 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? (3)
3 later devices cite it directly; ranked here by how many devices descend from each in turn.
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, K063851 (Vascular Solutions, Inc., 2007) has gone furthest, with 1 descendant of its own.
How does its category compare?
All KYX devicesKYX Dispenser, Liquid Medication: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KYX
1in 2015
2026 to Oct 25, outlined.
Median 510(k) review, days · KYX
Too few KYX 510(k)s in any year since 2007 to give a median.
Recalls per year · KYX
1in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KYX
11in 2025
MAUDE reports naming product code KYX, 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 | 3 |
| 2008 | 0 | — | 0 | 4 |
| 2009 | 0 | — | 0 | 7 |
| 2010 | 0 | — | 0 | 6 |
| 2011 | 0 | — | 2 | 5 |
| 2012 | 0 | — | 0 | 6 |
| 2013 | 0 | — | 0 | 4 |
| 2014 | 0 | — | 1 | 1 |
| 2015 | 1 | — | 0 | 11 |
| 2016 | 0 | — | 0 | 9 |
| 2017 | 0 | — | 0 | 17 |
| 2018 | 0 | — | 0 | 17 |
| 2019 | 0 | — | 0 | 17 |
| 2020 | 0 | — | 0 | 33 |
| 2021 | 0 | — | 0 | 7 |
| 2022 | 0 | — | 1 | 11 |
| 2023 | 0 | — | 0 | 31 |
| 2024 | 0 | — | 0 | 20 |
| 2025 | 0 | — | 0 | 11 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K792227 · printed Nov 6, 2026
Cite this page
510(k) Report. “K792227: Multi-AD Fluid Dispensing System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K792227
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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