# K241372: Advisor™ HD Grid X Mapping Catheter, Sensor Enabled™

- Pathway: 510(k) (Special)
- Applicant: Abbott Medical
- Decided: Jul 9, 2024 after 55 days
- Product code: MTD (Catheter, Intracardiac Mapping, High-Density Array)
- Device class: 2
- Regulation: 21 CFR 870.1220
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K983171 (1999). 17 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172393: Advisor HD Grid Mapping Catheter, Sensor Enabled, St. Jude Medical, Inc. (2018) Summary page 4.

## Most influential descendants
- K251211: ViewFlex™ Xtra ICE Catheter; ViewFlex™ Eco Reprocessed ICE Catheter; Advisor™ HD Grid Mapping Catheter, Sensor Enabled™; Advisor™ HD Grid X Mapping Catheter, Sensor Enabled™; Agilis™ NxT Steerable Introducer; Agilis™ NxT Steerable Introducer Dual-Reach™ (2025), 2 descendants of its own
- K250305: Reprocessed Agilis NxT Steerable Introducer (2026), 0 descendants of its own
- K250314: Medline ReNewal Reprocessed Abbott Agilis Nxt Steerable Introducer (2025), 0 descendants of its own

## Indications for use
The Advisor-M HD Grid X Mapping Catheter, Sensor EnabledT M , is indicated for multiple electrode electrophysiological mapping of cardiac structures in the heart, i.e., recording or stimulation only. This catheter is intended to obtain electrograms in the atrial and ventricular regions of the heart.

Source page: https://510kreport.com/device/K241372
Methodology: https://510kreport.com/methodology