510(k) Report

510(k) · Cleared

Cleared

CardioInsight Cardiac Mapping System

K181918510(k) TraditionalCleared Nov 8, 2018113-day reviewClass II21 CFR 870.1425

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Medtronic, Inc. · DQK Computer, Diagnostic, Programmable

Cleared on Nov 8, 2018 as substantially equivalent to K162440 (Cardioinsight Technologies, Inc., 2016) after a 113-day review. Its family tree reaches back 9 generations to 2000. 2 later devices descend from it.

Decided
Nov 8, 2018
Review
113 days
Class
Class II
Product code
DQK
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K000248 (2000). 16 ancestors in all, the oldest K874441 (1988). 2 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK000248 Carto EP Navigation SystemBiosense Webster, Inc. · 2000
  2. 5 generations between
  3. 3 generations backK140497 Ecvue Mapping SystemCardioinsight Technologies, Inc. · 2014
  4. 2 generations backK150990 ECVUE Mapping SystemCardioinsight Technologies, Inc. · 2015
  5. 1 generation backK162440 CardioInsight Cardiac Mapping SystemCardioinsight Technologies, Inc. · 2016
  6. This deviceK181918 CardioInsight Cardiac Mapping SystemMedtronic, Inc. · 2018
  7. Descendant · cites it directly · 1 of its ownK211546 Vektor Computational ECG Mapping System (vMap)Vektor Medical, Inc. · 2021
  8. Descendant · 2 generations on · 0 of its ownK252429 Vektor Computational ECG Mapping System (vMap®)Vektor Medical, Inc. · 2025
Show all 9 generations
  1. Root · 9 generations backK000248 Carto EP Navigation SystemBiosense Webster, Inc. · 2000
  2. 8 generations backK013083 Carto XP EP Navigation SystemBiosense Webster, Inc. · 2001
  3. 7 generations backK020863 Carto XP and Qwikmap EP Navigation SystemBiosense Webster, Inc. · 2003
  4. 6 generations backK042999 Carto XP EP Navigation System, Software Verison 8Biosense Webster, Inc. · 2005
  5. 5 generations backK101331 Labsystem Pro EP Recording System V3.1 SoftwareC.R. Bard Inc., Bard Electrophysiology Division · 2010
  6. 4 generations backK113811 V2.6 Software for the Labsystem Pro EP Recording SystemC.R. Bard Inc., Bard Electrophysiology Division · 2012
  7. 3 generations backK140497 Ecvue Mapping SystemCardioinsight Technologies, Inc. · 2014
  8. 2 generations backK150990 ECVUE Mapping SystemCardioinsight Technologies, Inc. · 2015
  9. 1 generation backK162440 CardioInsight Cardiac Mapping SystemCardioinsight Technologies, Inc. · 2016
  10. This deviceK181918 CardioInsight Cardiac Mapping SystemMedtronic, Inc. · 2018

Most influential descendants

Showing 2 of 2 · See all
  • K211546Vektor Computational ECG Mapping System (vMap)Vektor Medical, Inc. · 2021 · cites it directly1descendant
  • K252429Vektor Computational ECG Mapping System (vMap®)Vektor Medical, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K000248Carto EP Navigation SystemBiosense Webster, Inc.2000—
−8K013083Carto XP EP Navigation SystemBiosense Webster, Inc.2001—
−7K020863Carto XP and Qwikmap EP Navigation SystemBiosense Webster, Inc.2003—
−6K042999Carto XP EP Navigation System, Software Verison 8Biosense Webster, Inc.2005—
−5K101331Labsystem Pro EP Recording System V3.1 SoftwareC.R. Bard Inc., Bard Electrophysiology Division2010—
−4K113811V2.6 Software for the Labsystem Pro EP Recording SystemC.R. Bard Inc., Bard Electrophysiology Division2012—
−3K140497Ecvue Mapping SystemCardioinsight Technologies, Inc.2014—
−2K150990ECVUE Mapping SystemCardioinsight Technologies, Inc.2015—
−1K162440CardioInsight Cardiac Mapping SystemCardioinsight Technologies, Inc.2016—
0 (this device)K181918CardioInsight Cardiac Mapping SystemMedtronic, Inc.2018—
+1K211546Vektor Computational ECG Mapping System (vMap)Vektor Medical, Inc.2021—
+2K252429Vektor Computational ECG Mapping System (vMap®)Vektor Medical, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198820
199010
200010
200210
200320

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202510
FIG. 1 — Lineage of K181918, 2000–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 DQK? 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 DQK device

  1. #1 K213682 HemoSphere Advanced Monitor, HemoSphere…score 26.6 · 28 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K162440CardioInsight Cardiac Mapping System
Summary page 4
…Class II Panel: Cardiovascular Product Code: DQK Regulation: 21 CFR 870.1425 Predicate Device: CardioInsight Cardiac Mapping System, K162440, Cleared November 4, 2016 Page 1 of 5…
Cardioinsight Technologies, Inc.2016—

Also cleared against K162440: 2 other devices →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K211546Vektor Computational ECG Mapping System (vMap)Vektor Medical, Inc.20211

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 18 years and passes through 4 companies; a new generation was cleared every 1.5 years on median.
  • 1 of the 16 ancestors has a recall of any class.
  • Of its descendants, K211546 (Vektor Medical, Inc., 2021) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K162440.

How does its category compare?

All DQK devices

DQK Computer, Diagnostic, Programmable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · DQK

23so far in 2026, the most since 2007

2007: 132008: 42009: 122010: 92011: 122012: 72013: 132014: 92015: 72016: 152017: 72018: 142019: 152020: 162021: 162022: 192023: 212024: 132025: 222026 (partial year): 23
2007high 23 (2026) · low 4 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DQK

95in 2025

2007: 83 days median2008: 70 days median2009: 93 days median2010: 64 days median2011: 69 days median2012: 74 days median2013: 68 days median2014: 90 days median2015: 125 days median2016: 190 days median2017: 146 days median2018: 150 days median2019: 113 days median2020: 123 days median2021: 132 days median2022: 136 days median2023: 133 days median2024: 100 days median2025: 95 days median2026 (partial year): 151 days median
2007high 190 (2016) · low 64 (2010)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DQK

1in 2025

2007: 42008: 12009: 22010: 32011: 22012: 32013: 12014: 42015: 22017: 22018: 62019: 12020: 12021: 12022: 22023: 22024: 242025: 12026 (partial year): 2
2007high 24 (2024) · low 0 (2016)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DQK

433in 2025

2007: 182008: 342009: 402010: 492011: 552012: 1292013: 1802014: 1152015: 1312016: 3402017: 2522018: 2612019: 2182020: 2152021: 3512022: 3192023: 3402024: 5572025: 433
2007high 557 (2024) · low 18 (2007)2025

MAUDE reports naming product code DQK, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071383418
2008470134
20091293240
2010964349
20111269255
20127743129
201313681180
20149904115
201571252131
2016151900340
201771462252
2018141506261
2019151131218
2020161231215
2021161321351
2022191362319
2023211332340
20241310024557
202522951433
2026231512—

What is it indicated for?

The CardioInsight Cardiac Mapping System is intended for acquisition, analysis, display and storage of cardiac electrophysiological data and maps for analysis by a physician.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K181918: CardioInsight Cardiac Mapping System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K181918

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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