510(k) · Cleared
Recalled · Class II · 2015Micro-Temp Pumps & Micro-Temp Pads
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Seabrook Medical Systems, Inc. · ILO Pack, Hot Or Cold, Water Circulating
Cleared on Aug 17, 1984 after a 7-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it. It has been recalled 2 times.
- Decided
- Aug 17, 1984
- Review
- 7 days
- Class
- Class II
- Product code
- ILO
- Recalls
- 2
- Predicates
- 0
2 later devices descend from it, 1 citing it directly.
- This deviceK843146 Micro-Temp Pumps & Micro-Temp PadsSeabrook Medical Systems, Inc. · 1984
- Descendant · cites it directly · 1 of its ownK963293 Augustine Medical Wound Care System Model 68XXXAugustine Medical, Inc. · 1997
- Descendant · 2 generations on · 0 of its ownK020077 Modification to Augustine Medical Wound Care System, Model 68XXXAugustine Medical, Inc. · 2002
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K843146 | Micro-Temp Pumps & Micro-Temp Pads | Seabrook Medical Systems, Inc. | 1984 | — |
| +1 | K963293 | Augustine Medical Wound Care System Model 68XXX | Augustine Medical, Inc. | 1997 | — |
| +2 | K020077 | Modification to Augustine Medical Wound Care System, Model 68XXX | Augustine Medical, Inc. | 2002 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 2002 | 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 ILO? 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 ILO device
- #1 K213097 Armory Motionscore 4.7 · 5 generations · no Class I recall
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? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K963293 | Augustine Medical Wound Care System Model 68XXX | 1997 | 1 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jan 7, 2015 | Class II | Z-1129-2015 | Process design | Seals in the water path of the CT-99 cold therapy pad may separate during use, which could lead to a water leak. |
| Jan 18, 2005 | Not classified | Z-0671-05 | Other | There is the potential that the power switch assembly can dislodge from the cabinet during use. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K963293 (Augustine Medical, Inc., 1997) has gone furthest, with 1 descendant of its own.
How does its category compare?
All ILO devicesILO Pack, Hot Or Cold, Water Circulating: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · ILO
1in 2022
2026 to Oct 25, outlined.
Median 510(k) review, days · ILO
Too few ILO 510(k)s in any year since 2007 to give a median.
Recalls per year · ILO
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · ILO
9in 2025
MAUDE reports naming product code ILO, 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 | 2 | — | 0 | 14 |
| 2008 | 1 | — | 0 | 12 |
| 2009 | 1 | — | 2 | 17 |
| 2010 | 0 | — | 0 | 171 |
| 2011 | 0 | — | 1 | 241 |
| 2012 | 0 | — | 0 | 65 |
| 2013 | 0 | — | 8 | 60 |
| 2014 | 0 | — | 0 | 49 |
| 2015 | 0 | — | 0 | 60 |
| 2016 | 0 | — | 0 | 44 |
| 2017 | 0 | — | 1 | 43 |
| 2018 | 0 | — | 0 | 40 |
| 2019 | 0 | — | 0 | 29 |
| 2020 | 0 | — | 0 | 7 |
| 2021 | 0 | — | 1 | 14 |
| 2022 | 1 | — | 0 | 10 |
| 2023 | 0 | — | 0 | 12 |
| 2024 | 0 | — | 0 | 10 |
| 2025 | 0 | — | 0 | 9 |
| 2026 | 0 | — | 4 | — |
https://510kreport.com/device/K843146 · printed Nov 6, 2026
Cite this page
510(k) Report. “K843146: Micro-Temp Pumps & Micro-Temp Pads.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K843146
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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