510(k) · Cleared
ClearedCardioblate Maps Surgical Mapping, Ablation, Pacing and Sensing Device, Model 49205
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtronic · OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
Cleared on Jun 16, 2009 as substantially equivalent to K070288 (Medtronic Vascular, 2007) and 2 other predicates after a 90-day review. Its family tree reaches back 10 generations to 1995. 1 later device descends from it.
- Decided
- Jun 16, 2009
- Review
- 90 days
- Class
- Class II
- Product code
- OCL
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 10 generations to K942299 (1995). 65 ancestors in all, the oldest K811390 (1981). 1 later device descends from it, 1 citing it directly.
- Root · 10 generations backK942299 Endocare Cryotherapy SystemCytocare, Inc. · 1995
- 6 generations between
- 3 generations backK040641 Ultracinch Ablation Device, Ultracinch Accessory Pack, Models UC-8…Epicor Medical, Inc. · 2004
- 2 generations backK043579 Atricure Bipolar SystemAtriCure, Inc. · 2007
- 1 generation backK080509 Cardioblate 68000 Gnerator, BP2 Surgical Ablation Device, LP…Medtronic, Inc. · 2008
- This deviceK090721 Cardioblate Maps Surgical Mapping, Ablation, Pacing and Sensing…Medtronic · 2009
- Descendant · cites it directly · 0 of its ownK121451 Cardioblate Maps Surgical Mapping, Ablation, Pacing , and Sensing…Medtronic, Inc. · 2012
Show all 10 generations
- Root · 10 generations backK942299 Endocare Cryotherapy SystemCytocare, Inc. · 1995
- 9 generations backK963826 Endocare Crycare Cryosurgical SystemEndocare, Inc. · 1996
- 8 generations backK973686 Endocare Cryocare Cryosurgical SystemEndocare, Inc. · 1997
- 7 generations backK980110 Endocre Cryocare Cryosurgical SystemEndocare, Inc. · 1998
- 6 generations backK011722 Atricure Bipolar Coagulation SystemAtriCure, Inc. · 2001
- 5 generations backK020919 Atricure Bipolar System, Models ASU1, ASU2, ASU3, LHP1, LHP2, RHP1AtriCure, Inc. · 2002
- 4 generations backK022894 Epicor Medical Ablation SystemEpicor Medical, Inc. · 2004
- 3 generations backK040641 Ultracinch Ablation Device, Ultracinch Accessory Pack, Models UC-8…Epicor Medical, Inc. · 2004
- 2 generations backK043579 Atricure Bipolar SystemAtriCure, Inc. · 2007
- 1 generation backK080509 Cardioblate 68000 Gnerator, BP2 Surgical Ablation Device, LP…Medtronic, Inc. · 2008
- This deviceK090721 Cardioblate Maps Surgical Mapping, Ablation, Pacing and Sensing…Medtronic · 2009
Most influential descendants
Showing 1 of 1 · See all- K121451Cardioblate Maps Surgical Mapping, Ablation, Pacing , and Sensing DeviceMedtronic, Inc. · 2012 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K942299 | Endocare Cryotherapy System | Cytocare, Inc. | 1995 | — |
| −9 | K963826 | Endocare Crycare Cryosurgical System | Endocare, Inc. | 1996 | — |
| −8 | K973686 | Endocare Cryocare Cryosurgical System | Endocare, Inc. | 1997 | — |
| −7 | K980110 | Endocre Cryocare Cryosurgical System | Endocare, Inc. | 1998 | — |
| −6 | K011722 | Atricure Bipolar Coagulation System | AtriCure, Inc. | 2001 | — |
| −5 | K020919 | Atricure Bipolar System, Models ASU1, ASU2, ASU3, LHP1, LHP2, RHP1 | AtriCure, Inc. | 2002 | — |
| −4 | K022894 | Epicor Medical Ablation System | Epicor Medical, Inc. | 2004 | — |
| −3 | K040641 | Ultracinch Ablation Device, Ultracinch Accessory Pack, Models UC-8, UC-9… | Epicor Medical, Inc. | 2004 | — |
| −2 | K043579 | Atricure Bipolar System | AtriCure, Inc. | 2007 | — |
| −1 | K080509 | Cardioblate 68000 Gnerator, BP2 Surgical Ablation Device, LP Surgical Ablation… | Medtronic, Inc. | 2008 | — |
| 0 (this device) | K090721 | Cardioblate Maps Surgical Mapping, Ablation, Pacing and Sensing Device, Model… | Medtronic | 2009 | — |
| +1 | K121451 | Cardioblate Maps Surgical Mapping, Ablation, Pacing , and Sensing Device | Medtronic, Inc. | 2012 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1981 | 1 | 0 |
| 1987 | 1 | 0 |
| 1988 | 1 | 0 |
| 1991 | 1 | 0 |
| 1992 | 2 | 0 |
| 1994 | 1 | 0 |
| 1995 | 4 | 0 |
| 1996 | 1 | 0 |
| 1997 | 8 | 0 |
| 1998 | 5 | 0 |
| 1999 | 3 | 0 |
| 2000 | 4 | 0 |
| 2001 | 7 | 0 |
| 2002 | 5 | 0 |
| 2003 | 4 | 0 |
| 2004 | 3 | 0 |
| 2005 | 2 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 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 OCL? 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 OCL device
- #1 K252056 Isolator® Synergy™ EnCompass Clamp and Guide…score 13.0 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K070288 | Cardioblate Monopolar Pen, 60813, Cardioblate Monopolar XL, 60814Summary page 2…ating heart). Effects of this type of ablation have not been studied. Predicate Device 1 Medtronic Cardioblate® Monopolar Pen K070288 (cleared June 18, 2007), K080509 (cleared May 5, 2008); Reg 878.4400, Product Code: OCL… | 2007 |
| * | K080509 | Cardioblate 68000 Gnerator, BP2 Surgical Ablation Device, LP Surgical Ablation Device…Summary page 1…polar, radiofrequency ablation device powered by the Cardioblate® 68000 Generator (cleared via K060400, K080509). It has a saline irrigation system that delivers fluid at the contact point between tissue… | 2008 |
| * | K040812 | Detect Surgical Pacing and Mapping ToolSummary page 2…hen connected to a temporary external cardiac pacemaker. Predicate Device 2 Medtronic Detect Surgical Pacing and Mapping Tool K040812, cleared September 2, 2004, Reg 870.3680, Product Code: LDF Predicate Indications: The… | 2004 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K121451 | Cardioblate Maps Surgical Mapping, Ablation, Pacing , and Sensing Device | 2012 | 0 |
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 14 years and passes through 6 companies; a new generation was cleared every 1.1 years on median.
- 5 of the 65 ancestors have a recall of any class.
- Of its descendants, K121451 (Medtronic, Inc., 2012) has gone furthest, with 0 descendants of its own.
How does its category compare?
All OCL devicesOCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.
FDA decisions per year · OCL
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OCL
85in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OCL
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OCL
46in 2025
MAUDE reports naming product code OCL, 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 | 3 | 139 | 0 | 0 |
| 2008 | 5 | 81 | 1 | 0 |
| 2009 | 2 | — | 1 | 8 |
| 2010 | 2 | — | 2 | 23 |
| 2011 | 2 | — | 0 | 21 |
| 2012 | 6 | 75 | 0 | 21 |
| 2013 | 2 | — | 1 | 13 |
| 2014 | 1 | — | 0 | 15 |
| 2015 | 0 | — | 0 | 31 |
| 2016 | 0 | — | 1 | 76 |
| 2017 | 1 | — | 0 | 55 |
| 2018 | 2 | — | 0 | 61 |
| 2019 | 6 | 85 | 4 | 49 |
| 2020 | 1 | — | 4 | 37 |
| 2021 | 2 | — | 1 | 63 |
| 2022 | 2 | — | 0 | 59 |
| 2023 | 0 | — | 0 | 99 |
| 2024 | 1 | — | 0 | 59 |
| 2025 | 1 | — | 0 | 46 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Medtronic Cardioblate® MAPS Surgical Mapping, Ablation, Pacing, and Sensing Device is a sterile, single use electrosurgery device intended to ablate cardiac tissue using radiofrequency energy when connected to the Cardioblate® 68000 Generator or for temporary cardiac pacing, sensing, recording, and stimulation during the evaluation of cardiac arrhythmias during surgery when connected to an external temporary cardiac pacemaker.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K090721 · printed Nov 5, 2026
Cite this page
510(k) Report. “K090721: Cardioblate Maps Surgical Mapping, Ablation, Pacing and Sensing Device, Model 49205.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K090721
Report an extraction error
Are you the manufacturer?
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