510(k) Report

FDA applicant

Medtronic Ablation Frontiers, LLC

Carlsbad, CA1 decision2011–20111 recall

FDA records 1 decision for Medtronic Ablation Frontiers, LLC (Carlsbad, CA) in 2011: 1 510(k) clearance. All are in product code DRF (Catheter, Electrode Recording, Or Probe…). 1 recall is linked to its devices.

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

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Medtronic Ablation Frontiers, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

1in 2015

2015: 1
2011high 1 (2015) · low 0 (2011)2026

Class I Class II/III not classified

FIG. 1 — Medtronic Ablation Frontiers, LLC by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medtronic Ablation Frontiers, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • DRFCatheter, Electrode Recording, Or Probe, Electrode Recording1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K102588Achieve Mapping Catheter and Electrical CableMedtronic Ablation Frontiers, LLC · 20111cites it

What has FDA decided for it lately?

  • K102588Achieve Mapping Catheter and Electrical CableMedtronic Ablation Frontiers, LLC · 20111 recall

The one decision as Medtronic Ablation Frontiers, LLC →

What has been recalled?

1 recall linked to its devices; the latest:

  • K102588Medtronic Achieve Cables, model 990066. The sterile, single use only Electrical Cable…Sep 29, 2015Class II