510(k) · Cleared
Recalled · 2005Sabratek 6060 Homerun Volumetric Infusion Pump
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sabratek Corp. · FRN Pump, Infusion
Cleared on Jul 19, 1994 after an 85-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 3 later devices descend from it. It has been recalled once.
- Decided
- Jul 19, 1994
- Review
- 85 days
- Class
- Class II
- Product code
- FRN
- Recalls
- 1
- Predicates
- 0
3 later devices descend from it, 3 citing it directly.
- This deviceK941984 Sabratek 6060 Homerun Volumetric Infusion PumpSabratek Corp. · 1994
- Descendant · cites it directly · 0 of its ownK980751 Sabratek 4040 Infusion PumpSabratek Corp. · 1999
- Descendant · cites it directly · 0 of its ownK981816 Cue Ambulatory Volumetric Infusion PumpBecton Dickinson Curlin, LLC · 1998 · Recalled
- Descendant · cites it directly · 0 of its ownK981776 Alexander Manufacturing CO. Battery Part Number MC146XAlexander Mfg. Co. · 1998
Most influential descendants
Showing 3 of 3 · See all- K980751Sabratek 4040 Infusion PumpSabratek Corp. · 1999 · cites it directly0descendants
- K981816Cue Ambulatory Volumetric Infusion PumpBecton Dickinson Curlin, LLC · 1998 · cites it directly0descendants
- K981776Alexander Manufacturing CO. Battery Part Number MC146XAlexander Mfg. Co. · 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) | K941984 | Sabratek 6060 Homerun Volumetric Infusion Pump | Sabratek Corp. | 1994 | — |
| +1 | K980751 | Sabratek 4040 Infusion Pump | Sabratek Corp. | 1999 | — |
| +1 | K981816 | Cue Ambulatory Volumetric Infusion Pump | Becton Dickinson Curlin, LLC | 1998 | 56 |
| +1 | K981776 | Alexander Manufacturing CO. Battery Part Number MC146X | Alexander Mfg. Co. | 1998 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 2 | 0 |
| 1999 | 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 FRN? 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 FRN device
- #1 K253703 RemunityPRO+ Pump for Remodulin®…score 12.6 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA lists a 510(k) statement for it but has not posted the file, 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)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Aug 17, 2005 | Not classified | Z-1592-05 | Other | Potential overinfusion in the Auto-Ramp mode with software versions 3.00 or higher |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K980751 (Sabratek Corp., 1999) has gone furthest, with 0 descendants of its own.
How does its category compare?
All FRN devicesFRN Pump, Infusion: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FRN
8in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FRN
172in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FRN
7in 2025
Class I (37 since 2007) Class II/III not classified
Adverse event reports per year · FRN
52,792in 2025
MAUDE reports naming product code FRN, 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 | 12 | 102 | 15 | 1,086 |
| 2008 | 8 | 89 | 24 | 8,261 |
| 2009 | 9 | 66 | 102 | 1,952 |
| 2010 | 3 | 93 | 37 | 6,133 |
| 2011 | 3 | 103 | 69 | 41,367 |
| 2012 | 4 | 217 | 42 (2) | 15,482 |
| 2013 | 6 | 312 | 22 (3) | 40,082 |
| 2014 | 6 | 172 | 4 (3) | 94,180 |
| 2015 | 3 | 232 | 5 | 26,742 |
| 2016 | 3 | 301 | 7 (1) | 16,560 |
| 2017 | 3 | 305 | 13 | 12,060 |
| 2018 | 3 | 267 | 1 | 16,591 |
| 2019 | 2 | — | 18 (1) | 15,850 |
| 2020 | 1 | — | 16 (5) | 94,186 |
| 2021 | 2 | — | 3 (2) | 199,342 |
| 2022 | 6 | 268 | 2 | 888,020 |
| 2023 | 7 | 265 | 16 (10) | 165,838 |
| 2024 | 5 | 103 | 9 (4) | 57,730 |
| 2025 | 8 | 172 | 7 (4) | 52,792 |
| 2026 | 2 | — | 11 (2) | — |
https://510kreport.com/device/K941984 · printed Nov 6, 2026
Cite this page
510(k) Report. “K941984: Sabratek 6060 Homerun Volumetric Infusion Pump.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K941984
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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