510(k) · Cleared
ClearedCardioFlux with Faraday Analytical Cloud
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Genetesis, Inc. · DPS Electrocardiograph
Cleared on Mar 15, 2019 as substantially equivalent to K151135 (Tristan Technologies, Inc., 2016) after a 178-day review. Its family tree reaches back 4 generations to 1990.
- Decided
- Mar 15, 2019
- Review
- 178 days
- Class
- Class II
- Product code
- DPS
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K901215 (1990). 5 ancestors in all, the oldest K760542 (1976). No later device cites it as a predicate yet.
- Root · 4 generations backK901215 700 Series BiomagnetometerBiomagnetic Technologies, Inc. · 1990
- 3 generations backK962764 Neuromag-122Philips Medical Systems (Cleveland), Inc. · 1996
- 2 generations backK033488 Cmi MagnetocardiographCmi Cardiomag Imaging, Inc. · 2004
- 1 generation backK151135 Model 621/624 BiomagnetometerTristan Technologies, Inc. · 2016
- This deviceK182571 CardioFlux with Faraday Analytical CloudGenetesis, Inc. · 2019
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K901215 | 700 Series Biomagnetometer | Biomagnetic Technologies, Inc. | 1990 | — |
| −3 | K962764 | Neuromag-122 | Philips Medical Systems (Cleveland), Inc. | 1996 | — |
| −2 | K033488 | Cmi Magnetocardiograph | Cmi Cardiomag Imaging, Inc. | 2004 | — |
| −1 | K151135 | Model 621/624 Biomagnetometer | Tristan Technologies, Inc. | 2016 | — |
| 0 (this device) | K182571 | CardioFlux with Faraday Analytical Cloud | Genetesis, Inc. | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1976 | 1 | 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 DPS? 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 DPS device
- #1 K212112 Cardiologs Holter Platformscore 18.6 · 5 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 |
|---|---|---|---|
| * | K151135 | Model 621/624 BiomagnetometerSummary page 4…netocardiograph COMMON NAME: Magnetocardiograph DEVICE CLASS: Class II CLASSIFICATION NAME: Electrocardiograph (21 CFR 870.2340) PRODUCT CODE: DPS PREDICATE DEVICE(S): K151135 Tristan Technologies Model 621/624 Biomagnetometer DEVICE DESCRIPTION: The CardioFlux FAC Magnetocardiograph (MCG) is a biomagn… | 2016 |
What descends from it?
No later submission names this one as a predicate yet.
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 29 years and passes through 5 companies; a new generation was cleared every 7.7 years on median.
- None of the 5 ancestors has a recall.
How does its category compare?
All DPS devicesDPS Electrocardiograph: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · DPS
6in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DPS
163in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DPS
3in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · DPS
55in 2025
MAUDE reports naming product code DPS, 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 | 11 | 87 | 2 | 9 |
| 2008 | 13 | 31 | 0 | 17 |
| 2009 | 14 | 84 | 1 | 14 |
| 2010 | 11 | 104 | 2 | 21 |
| 2011 | 22 | 154 | 1 | 121 |
| 2012 | 12 | 117 | 0 | 56 |
| 2013 | 10 | 134 | 0 | 15 |
| 2014 | 11 | 253 | 0 | 15 |
| 2015 | 8 | 178 | 0 | 30 |
| 2016 | 11 | 229 | 0 | 12 |
| 2017 | 9 | 177 | 0 | 15 |
| 2018 | 14 | 221 | 0 | 19 |
| 2019 | 3 | 178 | 9 | 27 |
| 2020 | 6 | 224 | 2 | 59 |
| 2021 | 5 | 135 | 1 | 24 |
| 2022 | 6 | 244 | 1 | 59 |
| 2023 | 10 | 236 | 3 | 54 |
| 2024 | 8 | 260 | 4 (1) | 64 |
| 2025 | 6 | 163 | 3 | 55 |
| 2026 | 6 | 258 | 4 | — |
What is it indicated for?
The CardioFlux FAC Magnetocardiograph is intended for use as a tool which non-invasively measures and displays the magnetic signals produced by the electric currents of the heart.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K182571 · printed Nov 4, 2026
Cite this page
510(k) Report. “K182571: CardioFlux with Faraday Analytical Cloud.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K182571
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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