# K090721: Cardioblate Maps Surgical Mapping, Ablation, Pacing and Sensing Device, Model 49205

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic
- Decided: Jun 16, 2009 after 90 days
- Product code: OCL (Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K942299 (1995). 65 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 67 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070288: Cardioblate Monopolar Pen, 60813, Cardioblate Monopolar XL, 60814, Medtronic Vascular (2007) Summary page 2.
- K080509: Cardioblate 68000 Gnerator, BP2 Surgical Ablation Device, LP Surgical Ablation Device, Gemini-Ssurgical Ablation Device, Medtronic, Inc. (2008) Summary page 1.
- K040812: Detect Surgical Pacing and Mapping Tool, Medtronic Vascular (2004) Summary page 2.

## Most influential descendants
- K121451: Cardioblate Maps Surgical Mapping, Ablation, Pacing , and Sensing Device (2012), 0 descendants of its own

## Indications for use
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.

Source page: https://510kreport.com/device/K090721
Methodology: https://510kreport.com/methodology