510(k) · Cleared
ClearedElectrocardiograph
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Edan Instruments, Inc. · DPS Electrocardiograph
Cleared on Jun 2, 2017 as substantially equivalent to K152427 (Edan Instruments, Inc., 2016) and 1 other predicate after a 60-day review. Its family tree reaches back 10 generations to 1991. 3 later devices descend from it.
- Decided
- Jun 2, 2017
- Review
- 60 days
- Class
- Class II
- Product code
- DPS
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 10 generations to K903644 (1991). 38 ancestors in all, the oldest K820885 (1982). 3 later devices descend from it, 1 citing it directly.
- Root · 10 generations backK903644 Series 1500 12-Lead Analysis OptionMarquette Electronics, Inc. · 1991
- 6 generations between
- 3 generations backK131819 PC ECGEdan Instruments, Inc. · 2013
- 2 generations backK152427 PC ECGEdan Instruments, Inc. · 2016
- 1 generation backK160876 PC ECGEdan Instruments, Inc. · 2017
- This deviceK170995 ElectrocardiographEdan Instruments, Inc. · 2017
- Descendant · cites it directly · 2 of its ownK212278 ElectrocardiographEdan Instruments, Inc. · 2022
- Descendant · 2 generations on · 1 of its ownK222902 Electrocardiograph: SE-1200 Pro and SE-1201 ProEdan Instruments, Inc. · 2023
- Descendant · 3 generations on · 0 of its ownK232210 X-trodes System MX-Trodes · 2024
Show all 10 generations
- Root · 10 generations backK903644 Series 1500 12-Lead Analysis OptionMarquette Electronics, Inc. · 1991
- 9 generations backK973403 Cardiosmart STMarquette Medical Systems, Inc. · 1998
- 8 generations backK991014 Case 8000 Exercise Testing SystemGeneral Electric Medical Systems Information Techn · 1999
- 7 generations backK023380 T-Wave Altermans (Twa) Algorithm OptionGeneral Electric Medical Systems Information Techn · 2002
- 6 generations backK031561 Cardiosoft/Case Cardiac Testing SystemGe Medical Systems Information Technologies · 2003
- 5 generations backK092010 PC Ecg, Model SE-1010Edan Instruments, Inc. · 2009
- 4 generations backK102854 PC ECGEdan Instruments, Inc. · 2010
- 3 generations backK131819 PC ECGEdan Instruments, Inc. · 2013
- 2 generations backK152427 PC ECGEdan Instruments, Inc. · 2016
- 1 generation backK160876 PC ECGEdan Instruments, Inc. · 2017
- This deviceK170995 ElectrocardiographEdan Instruments, Inc. · 2017
Most influential descendants
Showing 3 of 3 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K903644 | Series 1500 12-Lead Analysis Option | Marquette Electronics, Inc. | 1991 | — |
| −9 | K973403 | Cardiosmart ST | Marquette Medical Systems, Inc. | 1998 | — |
| −8 | K991014 | Case 8000 Exercise Testing System | General Electric Medical Systems Information Techn | 1999 | — |
| −7 | K023380 | T-Wave Altermans (Twa) Algorithm Option | General Electric Medical Systems Information Techn | 2002 | — |
| −6 | K031561 | Cardiosoft/Case Cardiac Testing System | Ge Medical Systems Information Technologies | 2003 | — |
| −5 | K092010 | PC Ecg, Model SE-1010 | Edan Instruments, Inc. | 2009 | — |
| −4 | K102854 | PC ECG | Edan Instruments, Inc. | 2010 | — |
| −3 | K131819 | PC ECG | Edan Instruments, Inc. | 2013 | — |
| −2 | K152427 | PC ECG | Edan Instruments, Inc. | 2016 | — |
| −1 | K160876 | PC ECG | Edan Instruments, Inc. | 2017 | — |
| 0 (this device) | K170995 | Electrocardiograph | Edan Instruments, Inc. | 2017 | — |
| +1 | K212278 | Electrocardiograph | Edan Instruments, Inc. | 2022 | — |
| +2 | K222902 | Electrocardiograph: SE-1200 Pro and SE-1201 Pro | Edan Instruments, Inc. | 2023 | — |
| +3 | K232210 | X-trodes System M | X-Trodes | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1982 | 1 | 0 |
| 1989 | 1 | 0 |
| 1990 | 1 | 0 |
| 1993 | 1 | 0 |
| 1994 | 2 | 0 |
| 1996 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 2 | 0 |
| 1999 | 3 | 0 |
| 2000 | 1 | 0 |
| 2002 | 2 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 3 | 0 |
| 2007 | 1 | 0 |
| 2009 | 2 | 0 |
| 2010 | 2 | 0 |
| 2014 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2022 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 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? (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 |
|---|---|---|---|
| * | K152427 | PC ECGSummary page 4…PS Regulatory Class: Class II 3. Predicate Device(s): 1. EDAN Instrument, Inc. Electrocardiograph, models SE-1515, K152427 (Primary) 2. EDAN Instrument, Inc. Electrocardiograph, models SE-12, SE-12 Ex… | 2016 |
| * | K160876 | PC ECGSummary page 4…427 (Primary) 2. EDAN Instrument, Inc. Electrocardiograph, models SE-12, SE-12 Express, SE-1200, and SE-1200 Express, K160876 (Reference) 4. Reason for New model Submission 5. Pre-Submission, Not applicable, there is no prior submissio… | 2017 |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K212278 | Electrocardiograph | 2022 | 2 |
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 26 years and passes through 5 companies; a new generation was cleared every 2.2 years on median.
- 3 of the 38 ancestors have a recall of any class.
- Of its descendants, K212278 (Edan Instruments, Inc., 2022) has gone furthest, with 2 descendants of its own.
- 2 other devices also cite its predicate K152427.
How does its category compare?
All DPS devicesDPS Electrocardiograph: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, 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 SE-18 18-lead electrocardiograph is intended to acquire ECG signals from adult and pediatric patients through body surface ECG electrodes. The electrocardiograph is only intended to be used in hospitals or healthcare facilities by doctors and trained healthcare professionals. The cardiogram recorded by the electrocardiograph can help users to analyze and diagnose heart disease. However, the interpreted ECG with measurements and interpretive statements is offered to clinicians on an advisory basis only.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K170995 · printed Nov 6, 2026
Cite this page
510(k) Report. “K170995: Electrocardiograph.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K170995
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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