510(k) · Cleared
ClearedZoe Fluid Status Monitor
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Noninvasive Medical Technologies, Inc. · DSB Plethysmograph, Impedance
Cleared on Jun 28, 2013 as substantially equivalent to K112830 (Noninvasive Medical Technologies, Inc., 2012) after a 35-day review. Its family tree reaches back 3 generations to 1992. 18 later devices descend from it.
- Decided
- Jun 28, 2013
- Review
- 35 days
- Class
- Class II
- Product code
- DSB
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K922218 (1992). 4 ancestors in all. 18 later devices descend from it, 2 citing it directly.
- Root · 3 generations backK922218 IQ SystemRenaissance Technology, Inc. · 1992
- 2 generations backK042113 Zoe Fluid Status MonitorNoninvasive Medical Technologies, LLC · 2004
- 1 generation backK112830 Zoefluid Status Monitor (Model Zoe 2B)Noninvasive Medical Technologies, Inc. · 2012
- This deviceK131509 Zoe Fluid Status MonitorNoninvasive Medical Technologies, Inc. · 2013
- Descendant · cites it directly · 17 of its ownK133301 Zoe Fluid Status MonitorNoninvasive Medical Technologies, Inc. · 2014
- Descendant · 2 generations on · 10 of its ownK142503 Imed-Z Fluid Status MonitorIntersection Medical, Inc. · 2015
- Descendant · 3 generations on · 7 of its ownK172507 SOZOImpediMed Limited · 2017
- Descendant · 4 generations on · 4 of its ownK193410 SOZO Body Fluid AnalyzerImpediMed Limited · 2020
- Descendant · 5 generations on · 3 of its ownK203473 SOZOImpediMed Limited · 2021
Showing 5 of 18 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 18 · See all- K133301Zoe Fluid Status MonitorNoninvasive Medical Technologies, Inc. · 2014 · cites it directly17descendants
- K142503Imed-Z Fluid Status MonitorIntersection Medical, Inc. · 2015 · 2 generations on10descendants
- K172507SOZOImpediMed Limited · 2017 · 3 generations on7descendants
- K193410SOZO Body Fluid AnalyzerImpediMed Limited · 2020 · 4 generations on4descendants
- K203473SOZOImpediMed Limited · 2021 · 5 generations on3descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K922218 | IQ System | Renaissance Technology, Inc. | 1992 | — |
| −2 | K042113 | Zoe Fluid Status Monitor | Noninvasive Medical Technologies, LLC | 2004 | — |
| −1 | K112830 | Zoefluid Status Monitor (Model Zoe 2B) | Noninvasive Medical Technologies, Inc. | 2012 | — |
| 0 (this device) | K131509 | Zoe Fluid Status Monitor | Noninvasive Medical Technologies, Inc. | 2013 | — |
| +1 | K133301 | Zoe Fluid Status Monitor | Noninvasive Medical Technologies, Inc. | 2014 | — |
| +2 | K142503 | Imed-Z Fluid Status Monitor | Intersection Medical, Inc. | 2015 | — |
| +3 | K172507 | SOZO | ImpediMed Limited | 2017 | — |
| +4 | K193410 | SOZO Body Fluid Analyzer | ImpediMed Limited | 2020 | — |
| +5 | K203473 | SOZO | ImpediMed Limited | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1999 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2015 | 2 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 3 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 2 | 0 |
| 2025 | 3 | 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 DSB? 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 DSB device
- #1 K232089 SOZO Proscore 14.6 · 9 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
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 |
|---|---|---|---|
| * | K112830 | Zoefluid Status Monitor (Model Zoe 2B)Summary page 1…tially equivalent to the following currently marketed Predicate Device. Manufacturer Device Name 510-K Number Decision Date Noninvasive Medical ZOE Fluid Status Monitor K112830 11/13/2012 Technologies, Inc. Device Description: . The ZOE Fluid Status Monitor is a non-invasive; battery powered impedance mo… | 2012 |
What descends from it? (18)
See all 182 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?
- The line of descent spans 21 years and passes through 3 companies; a new generation was cleared every 8.2 years on median.
- None of the 4 ancestors has a recall.
- Of its descendants, K133301 (Noninvasive Medical Technologies, Inc., 2014) has gone furthest, with 17 descendants of its own.
- 2 other devices also cite its predicate K112830.
How does its category compare?
All DSB devicesDSB Plethysmograph, Impedance: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · DSB
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DSB
266in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DSB
1in 2015
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DSB
2in 2025
MAUDE reports naming product code DSB, 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 | 0 |
| 2008 | 6 | 90 | 0 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 0 |
| 2011 | 2 | — | 0 | 0 |
| 2012 | 1 | — | 0 | 0 |
| 2013 | 2 | — | 0 | 0 |
| 2014 | 2 | — | 0 | 0 |
| 2015 | 2 | — | 1 | 0 |
| 2016 | 0 | — | 0 | 1 |
| 2017 | 2 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 1 | — | 0 | 0 |
| 2020 | 2 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 0 |
| 2022 | 1 | — | 0 | 0 |
| 2023 | 2 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 3 | 266 | 0 | 2 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The ZOE Fluid Status Monitor is intended for patients
With fluid management problems
Taking diuretic medication
Living with Heart Failure
Living with End-stage Renal Disease
Recovering from Coronary Artery Disease related event
Suffering from Recurrent Dehydration
This device is intended for use under the direction of a physician, for the non-invasive monitoring and management of patients with fluid management problems in a variety of medically accepted clinical applications.
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/K131509 · printed Nov 6, 2026
Cite this page
510(k) Report. “K131509: Zoe Fluid Status Monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131509
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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