510(k) Report

510(k) · Cleared

Cleared

Affera Integrated Mapping System; Impedance Localization Patch Kit

K241828510(k) TraditionalCleared Nov 1, 2024130-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 1, 2024 as substantially equivalent to K233943 (Medtronic, Inc., 2024) and 1 other predicate after a 130-day review. Its family tree reaches back 18 generations to 2000. 4 later devices descend from it.

Decided
Nov 1, 2024
Review
130 days
Class
Class II
Product code
DQK
Recalls
None
Predicates
2

Its longest line of descent runs back 18 generations to K001437 (2000). 59 ancestors in all, the oldest K954395 (1995). 4 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2020: 1 other ancestor2018: 3 other ancestors2016: 3 other ancestors2015: 1 other ancestor2014: 1 other ancestor2013: 3 other ancestors2012: 1 other ancestor2011: 2 other ancestors2010: 6 other ancestors2008: 1 other ancestor2005: 3 other ancestors2009: 2 other ancestors2007: 1 other ancestor2006: 4 other ancestors2003: 1 other ancestor2001: 1 other ancestor2000: 3 other ancestors1999: 2 other ancestors1995: 1 other ancestor1998: 1 other ancestor2024: 1 descendant cleared2025: 2 descendants cleared2026: 1 descendant clearedK001437 · Ensite 3000 System, Model EE3000 · Endocardial Solutions, Inc. · 2000K012926 · Modification to Ensite 3000 System, Model EE3000 · Endocardial Solutions, Inc. · 2001K030129 · Modification to Ensite 3000 System, Model EE3000 · Endocardial Solutions, Inc. · 2003K042493 · Ensite System, Model EE3000 · Endocardial Solutions, Inc. · 2004K060954 · Modification to Ensite System, Model EE3000 · St. Jude Medical, Inc.-Endocardial Solutions · 2006K072202 · Carto 3 Navigation System (Model:FG-5400-00), Carto 3 External Reference Patches (Model:D-1283-01) · Biosense Webster, Inc. · 2007×2: 2 generations cleared close together, K090017 (2009), K093455 (2009) K103746 · Carto 3 EP Navigation System, Version 2.0 (W/Standard Location Pad),CARTO3 Epnavigation System,Version 2.0 W/RMT Pad) · Biosense Webster, Inc. · 2011 · recalledK112007 · Carto 3 EP Navigation System, Version 2.2 · Biosense Webster, Inc. · 2011 · recalledK120550 · Carto (R) EP Navigation System, Version 3.0 (with Standard Location Pad) · Biosense Webster, Inc. · 2012 · recalledK133916 · Carto 3 EP Navigation System, Version 4.2 · Biosense Webster, Inc. · 2014 · recalledK170600 · CARTO 3 EP Navigation System, Version 6.0 and Accessories · Biosense Webster, Inc. · 2017K180238 · CARTO 3 EP Navigation System, Version 6.0 and Accessories with VISITAG SURPOINT · Biosense Webster, Inc. · 2018K191660 · CARTO 3 EP Navigation System, Version 7.1 and Accessories · Biosense Webster, Inc. · 2019 · recalledK200484 · CARTO® 3 EP Navigation System with Signal Processing Unit · Biosense Webster, Inc. · 2020K213264 · CARTO 3 EP Navigation System Version 7.2 · Biosense Webster, Inc. · 2021K233943 · Affera Mapping System (AFR-00003); Location Reference Patch Kit (AFR-00007); System Cart (AFR-00013) · Medtronic, Inc. · 20241995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor3 generations back: 1 other ancestor4 generations back: 1 other ancestor5 generations back: 3 other ancestors6 generations back: 8 other ancestors7 generations back: 7 other ancestors8 generations back: 4 other ancestors9 generations back: 2 other ancestors10 generations back: 10 other ancestors12 generations back: 1 other ancestor13 generations back: 2 other ancestors 1 generation forward: 3 descendants2 generations forward: 1 descendant K233943 · Affera Mapping System (AFR-00003); Location Reference Patch Kit (AFR-00007); System Cart (AFR-00013) · Medtronic, Inc. · 2024K213264 · CARTO 3 EP Navigation System Version 7.2 · Biosense Webster, Inc. · 2021K200484 · CARTO® 3 EP Navigation System with Signal Processing Unit · Biosense Webster, Inc. · 2020K191660 · CARTO 3 EP Navigation System, Version 7.1 and Accessories · Biosense Webster, Inc. · 2019 · recalledK180238 · CARTO 3 EP Navigation System, Version 6.0 and Accessories with VISITAG SURPOINT · Biosense Webster, Inc. · 2018K170600 · CARTO 3 EP Navigation System, Version 6.0 and Accessories · Biosense Webster, Inc. · 2017K133916 · Carto 3 EP Navigation System, Version 4.2 · Biosense Webster, Inc. · 2014 · recalledK120550 · Carto (R) EP Navigation System, Version 3.0 (with Standard Location Pad) · Biosense Webster, Inc. · 2012 · recalledK112007 · Carto 3 EP Navigation System, Version 2.2 · Biosense Webster, Inc. · 2011 · recalledK103746 · Carto 3 EP Navigation System, Version 2.0 (W/Standard Location Pad),CARTO3 Epnavigation System,Version 2.0 W/RMT Pad) · Biosense Webster, Inc. · 2011 · recalledK093455 · Carto 3 Version 1.05 EP Navigation System and Accessories · Biosense Webster, Inc. · 2009 · recalledK090017 · Carto 3 EP Navigation System, V1.0 and Accessories · Biosense Webster, Inc. · 2009 · recalledK072202 · Carto 3 Navigation System (Model:FG-5400-00), Carto 3 External Reference Patches (Model:D-1283-01) · Biosense Webster, Inc. · 2007K060954 · Modification to Ensite System, Model EE3000 · St. Jude Medical, Inc.-Endocardial Solutions · 2006K042493 · Ensite System, Model EE3000 · Endocardial Solutions, Inc. · 2004K030129 · Modification to Ensite 3000 System, Model EE3000 · Endocardial Solutions, Inc. · 2003K012926 · Modification to Ensite 3000 System, Model EE3000 · Endocardial Solutions, Inc. · 2001K001437 · Ensite 3000 System, Model EE3000 · Endocardial Solutions, Inc. · 2000−15−10−50
  1. Root · 18 generations backK001437 Ensite 3000 System, Model EE3000Endocardial Solutions, Inc. · 2000
  2. 14 generations between
  3. 3 generations backK200484 CARTO® 3 EP Navigation System with Signal Processing UnitBiosense Webster, Inc. · 2020
  4. 2 generations backK213264 CARTO 3 EP Navigation System Version 7.2Biosense Webster, Inc. · 2021
  5. 1 generation backK233943 Affera Mapping System (AFR-00003); Location Reference Patch Kit…Medtronic, Inc. · 2024
  6. This deviceK241828 Affera Integrated Mapping System; Impedance Localization Patch KitMedtronic, Inc. · 2024
  7. Descendant · cites it directly · 1 of its ownK243892 Affera Integrated Mapping SystemMedtronic, Inc. · 2025
  8. Descendant · 2 generations on · 0 of its ownK262005 Affera Integrated Mapping SystemMedtronic, Inc. · 2026
  9. Descendant · cites it directly · 0 of its ownK250747 Globe® Pulsed Field SystemKardium, Inc. · 2025
  10. Descendant · cites it directly · 0 of its ownK243435 Magnetic Localization Patch Kit (AFR-00021)Medtronic, Inc. · 2024
Show all 18 generations
  1. Root · 18 generations backK001437 Ensite 3000 System, Model EE3000Endocardial Solutions, Inc. · 2000
  2. 17 generations backK012926 Modification to Ensite 3000 System, Model EE3000Endocardial Solutions, Inc. · 2001
  3. 16 generations backK030129 Modification to Ensite 3000 System, Model EE3000Endocardial Solutions, Inc. · 2003
  4. 15 generations backK042493 Ensite System, Model EE3000Endocardial Solutions, Inc. · 2004
  5. 14 generations backK060954 Modification to Ensite System, Model EE3000St. Jude Medical, Inc.-Endocardial Solutions · 2006
  6. 13 generations backK072202 Carto 3 Navigation System (Model:FG-5400-00), Carto 3 External…Biosense Webster, Inc. · 2007
  7. 12 generations backK090017 Carto 3 EP Navigation System, V1.0 and AccessoriesBiosense Webster, Inc. · 2009 · Recalled
  8. 11 generations backK093455 Carto 3 Version 1.05 EP Navigation System and AccessoriesBiosense Webster, Inc. · 2009 · Recalled
  9. 10 generations backK103746 Carto 3 EP Navigation System, Version 2.0 (W/Standard Location…Biosense Webster, Inc. · 2011 · Recalled
  10. 9 generations backK112007 Carto 3 EP Navigation System, Version 2.2Biosense Webster, Inc. · 2011 · Recalled
  11. 8 generations backK120550 Carto (R) EP Navigation System, Version 3.0 (with Standard Location…Biosense Webster, Inc. · 2012 · Recalled
  12. 7 generations backK133916 Carto 3 EP Navigation System, Version 4.2Biosense Webster, Inc. · 2014 · Recalled
  13. 6 generations backK170600 CARTO 3 EP Navigation System, Version 6.0 and AccessoriesBiosense Webster, Inc. · 2017
  14. 5 generations backK180238 CARTO 3 EP Navigation System, Version 6.0 and Accessories with…Biosense Webster, Inc. · 2018
  15. 4 generations backK191660 CARTO 3 EP Navigation System, Version 7.1 and AccessoriesBiosense Webster, Inc. · 2019 · Recalled
  16. 3 generations backK200484 CARTO® 3 EP Navigation System with Signal Processing UnitBiosense Webster, Inc. · 2020
  17. 2 generations backK213264 CARTO 3 EP Navigation System Version 7.2Biosense Webster, Inc. · 2021
  18. 1 generation backK233943 Affera Mapping System (AFR-00003); Location Reference Patch Kit…Medtronic, Inc. · 2024
  19. This deviceK241828 Affera Integrated Mapping System; Impedance Localization Patch KitMedtronic, Inc. · 2024

Most influential descendants

Showing 4 of 4 · See all
  • K243892Affera Integrated Mapping SystemMedtronic, Inc. · 2025 · cites it directly1descendant
  • K262005Affera Integrated Mapping SystemMedtronic, Inc. · 2026 · 2 generations on0descendants
  • K250747Globe® Pulsed Field SystemKardium, Inc. · 2025 · cites it directly0descendants
  • K243435Magnetic Localization Patch Kit (AFR-00021)Medtronic, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−18K001437Ensite 3000 System, Model EE3000Endocardial Solutions, Inc.2000—
−17K012926Modification to Ensite 3000 System, Model EE3000Endocardial Solutions, Inc.2001—
−16K030129Modification to Ensite 3000 System, Model EE3000Endocardial Solutions, Inc.2003—
−15K042493Ensite System, Model EE3000Endocardial Solutions, Inc.2004—
−14K060954Modification to Ensite System, Model EE3000St. Jude Medical, Inc.-Endocardial Solutions2006—
−13K072202Carto 3 Navigation System (Model:FG-5400-00), Carto 3 External Reference…Biosense Webster, Inc.2007—
−12K090017Carto 3 EP Navigation System, V1.0 and AccessoriesBiosense Webster, Inc.20094
−11K093455Carto 3 Version 1.05 EP Navigation System and AccessoriesBiosense Webster, Inc.20091
−10K103746Carto 3 EP Navigation System, Version 2.0 (W/Standard Location Pad),CARTO3…Biosense Webster, Inc.20111
−9K112007Carto 3 EP Navigation System, Version 2.2Biosense Webster, Inc.20112
−8K120550Carto (R) EP Navigation System, Version 3.0 (with Standard Location Pad)Biosense Webster, Inc.20122
−7K133916Carto 3 EP Navigation System, Version 4.2Biosense Webster, Inc.20142
−6K170600CARTO 3 EP Navigation System, Version 6.0 and AccessoriesBiosense Webster, Inc.2017—
−5K180238CARTO 3 EP Navigation System, Version 6.0 and Accessories with VISITAG SURPOINTBiosense Webster, Inc.2018—
−4K191660CARTO 3 EP Navigation System, Version 7.1 and AccessoriesBiosense Webster, Inc.20191
−3K200484CARTO® 3 EP Navigation System with Signal Processing UnitBiosense Webster, Inc.2020—
−2K213264CARTO 3 EP Navigation System Version 7.2Biosense Webster, Inc.2021—
−1K233943Affera Mapping System (AFR-00003); Location Reference Patch Kit (AFR-00007)…Medtronic, Inc.2024—
0 (this device)K241828Affera Integrated Mapping System; Impedance Localization Patch KitMedtronic, Inc.2024—
+1K243892Affera Integrated Mapping SystemMedtronic, Inc.2025—
+2K262005Affera Integrated Mapping SystemMedtronic, Inc.2026—
+1K250747Globe® Pulsed Field SystemKardium, Inc.2025—
+1K243435Magnetic Localization Patch Kit (AFR-00021)Medtronic, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199810
199920
200030
200110
200310
200530
200640
200710
200810
200920
201060
201120
201210
201330
201410
201510
201630
201830
202010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202520
202610
FIG. 1 — Lineage of K241828, 2000–2026Source: 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K233943Affera Mapping System (AFR-00003); Location Reference Patch Kit (AFR-00007); System Cart…
Summary page 5
…425, Cardiovascular Product Code: DQK Predicate Devices: • Affera Integrated Mapping System: Affera Mapping System – K233943 • Impedance Localization Patch Kit: EnSite Precision Surface Electrode…
Medtronic, Inc.2024—
*K201148EnSite Precision Cardiac Mapping System v2.6, EnSite Precision Software Installation…
Summary page 5
…System – K233943 • Impedance Localization Patch Kit: EnSite Precision Surface Electrode Kit – K201148 Device Description: Affera Integrated Mapping System The Affera Integrated Mapping System (integ…
Abbott Medical2020—

What descends from it? (4)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K243892Affera Integrated Mapping SystemMedtronic, Inc.20251
K250747Globe® Pulsed Field SystemKardium, Inc.20250
K243435Magnetic Localization Patch Kit (AFR-00021)Medtronic, Inc.20240

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 24 years and passes through 4 companies; a new generation was cleared every 1.4 years on median.
  • 8 of the 59 ancestors have a recall of any class.
  • Of its descendants, K243892 (Medtronic, Inc., 2025) has gone furthest, with 1 descendant of its own.

How does its category compare?

All DQK devices

DQK Computer, Diagnostic, Programmable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, 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?

Affera Integrated Mapping System:

The Affera integrated mapping system is intended to be used for catheter-based cardiac electrophysiological mapping. The mapping system allows pacing and real-time visualization of compatible catheters as well as display of cardiac maps in multiple formats. The acquired patient signals, including body surface electrocardiograms and intracardiac electrograms, may also be recorded and displayed on the system’s display screen.

Impedance Localization Patch Kit:

Refer to the instructions for use accompanying the compatible electrophysiology catheter(s) used with the compatible mapping system for the specific indications for use.

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. “K241828: Affera Integrated Mapping System; Impedance Localization Patch Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K241828

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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