510(k) · Cleared
ClearedMinimed 407C Infusion Pump, Model 407C
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtronic Minimed · FRN Pump, Infusion
Cleared on Jun 23, 1999 after an 89-day review. The FDA summary names its predicate without a number. 19 later devices descend from it.
- Decided
- Jun 23, 1999
- Review
- 89 days
- Class
- Class II
- Product code
- FRN
- Recalls
- None
- Predicates
- 0
19 later devices descend from it, 1 citing it directly.
- This deviceK991013 Minimed 407C Infusion Pump, Model 407CMedtronic Minimed · 1999
- Descendant · cites it directly · 18 of its ownK040061 Medtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-407CMedtronic Minimed · 2004
- Descendant · 2 generations on · 17 of its ownK043600 Medtronic Micromed 407C Infusion Pump, Model MMT-407CMedtronic Minimed · 2005
- Descendant · 3 generations on · 16 of its ownK061110 Glucommander PlusCollaborativemed, LLC · 2006
- Descendant · 4 generations on · 13 of its ownK101344 G+ SystemGlytec, LLC (Formally Known AS Glucotec, Inc.) · 2010
- Descendant · 5 generations on · 12 of its ownK113853 G+ SystemGlytec, LLC · 2012
Showing 5 of 19 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 19 · See all- K040061Medtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-407CMedtronic Minimed · 2004 · cites it directly18descendants
- K043600Medtronic Micromed 407C Infusion Pump, Model MMT-407CMedtronic Minimed · 2005 · 2 generations on17descendants
- K061110Glucommander PlusCollaborativemed, LLC · 2006 · 3 generations on16descendants
- K101344G+ SystemGlytec, LLC (Formally Known AS Glucotec, Inc.) · 2010 · 4 generations on13descendants
- K113853G+ SystemGlytec, LLC · 2012 · 5 generations on12descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K991013 | Minimed 407C Infusion Pump, Model 407C | Medtronic Minimed | 1999 | — |
| +1 | K040061 | Medtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-407C | Medtronic Minimed | 2004 | — |
| +2 | K043600 | Medtronic Micromed 407C Infusion Pump, Model MMT-407C | Medtronic Minimed | 2005 | — |
| +3 | K061110 | Glucommander Plus | Collaborativemed, LLC | 2006 | — |
| +4 | K101344 | G+ System | Glytec, LLC (Formally Known AS Glucotec, Inc.) | 2010 | — |
| +5 | K113853 | G+ System | Glytec, LLC | 2012 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
| 2010 | 1 | 0 |
| 2012 | 1 | 0 |
| 2014 | 2 | 0 |
| 2015 | 1 | 0 |
| 2017 | 2 | 0 |
| 2018 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
| 2024 | 1 | 0 |
| 2026 | 2 | 0 |
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 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? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | MiniMed Model 507C Insulin Pump Named without a submission number | |
| * | — | MiniMed 404-SP Infusion Pump Named without a submission number |
What descends from it? (19)
See all 191 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K040061 | Medtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-407C | 2004 | 18 |
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, K040061 (Medtronic Minimed, 2004) has gone furthest, with 18 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) | — |
What is it indicated for?
The MiniMed 407C Infusion Pump is indicated for infusion of medication labeled for subcutancous administration, at sct and variable rates, for therapies including chemotherapy, antibiotic therapy, and controlled analgesia.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K991013 · printed Nov 5, 2026
Cite this page
510(k) Report. “K991013: Minimed 407C Infusion Pump, Model 407C.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K991013
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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