510(k) · Cleared
ClearedMedtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-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 Apr 8, 2004 as substantially equivalent to K991013 (Medtronic Minimed, 1999) after an 86-day review. Its family tree reaches back 1 generation to 1999. 18 later devices descend from it.
- Decided
- Apr 8, 2004
- Review
- 86 days
- Class
- Class II
- Product code
- FRN
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K991013 (1999). 18 later devices descend from it, 1 citing it directly.
- Root · 1 generation backK991013 Minimed 407C Infusion Pump, Model 407CMedtronic Minimed · 1999
- This deviceK040061 Medtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-407CMedtronic Minimed · 2004
- Descendant · cites it directly · 17 of its ownK043600 Medtronic Micromed 407C Infusion Pump, Model MMT-407CMedtronic Minimed · 2005
- Descendant · 2 generations on · 16 of its ownK061110 Glucommander PlusCollaborativemed, LLC · 2006
- Descendant · 3 generations on · 13 of its ownK101344 G+ SystemGlytec, LLC (Formally Known AS Glucotec, Inc.) · 2010
- Descendant · 4 generations on · 12 of its ownK113853 G+ SystemGlytec, LLC · 2012
- Descendant · 5 generations on · 8 of its ownK132547 Endo Tool Glucose Management System (Egms)Monarch Medical Technologies · 2014 · Recalled
Showing 5 of 18 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 18 · See all- K043600Medtronic Micromed 407C Infusion Pump, Model MMT-407CMedtronic Minimed · 2005 · cites it directly17descendants
- K061110Glucommander PlusCollaborativemed, LLC · 2006 · 2 generations on16descendants
- K101344G+ SystemGlytec, LLC (Formally Known AS Glucotec, Inc.) · 2010 · 3 generations on13descendants
- K113853G+ SystemGlytec, LLC · 2012 · 4 generations on12descendants
- K132547Endo Tool Glucose Management System (Egms)Monarch Medical Technologies · 2014 · 5 generations on8descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K991013 | Minimed 407C Infusion Pump, Model 407C | Medtronic Minimed | 1999 | — |
| 0 (this device) | K040061 | Medtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-407C | Medtronic Minimed | 2004 | — |
| +1 | K043600 | Medtronic Micromed 407C Infusion Pump, Model MMT-407C | Medtronic Minimed | 2005 | — |
| +2 | K061110 | Glucommander Plus | Collaborativemed, LLC | 2006 | — |
| +3 | K101344 | G+ System | Glytec, LLC (Formally Known AS Glucotec, Inc.) | 2010 | — |
| +4 | K113853 | G+ System | Glytec, LLC | 2012 | — |
| +5 | K132547 | Endo Tool Glucose Management System (Egms) | Monarch Medical Technologies | 2014 | 1 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 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 |
|---|---|---|---|
| * | K991013 | Minimed 407C Infusion Pump, Model 407CSummary page 1…own as the MicroMed 407C described in this submission are: The features of device that is the subject to this submission are identical to those of the predicate device (K991013). The only change is expansion of the indications for use to include intrathecal in fusion. This change to the indications for u… | 1999 |
| * | — | SIMS Deltec CADD-Micro, Model 5900 Named without a submission number |
What descends from it? (18)
See all 181 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K043600 | Medtronic Micromed 407C Infusion Pump, Model MMT-407C | 2005 | 17 |
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?
- Its one ancestor has no recall.
- Of its descendants, K043600 (Medtronic Minimed, 2005) has gone furthest, with 17 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 Medtronic MiniMed MicroMed 407C Drug Infusion Pump is indicated for infusion of medication labeled subcutaneous and intrathecal infusion. The pump is intended for therapies at set and variable rates, for therapies including, but not limited to chemotherapy, antibiotic therapy, and controlled analgesia.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K040061 · printed Nov 6, 2026
Cite this page
510(k) Report. “K040061: Medtronic Minimed MMT-407C Ambulatory Infusion Pump, Model MMT-407C.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K040061
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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