Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list RhythmLink International with 18 510(k) clearances. The most recent is a 510(k) clearance dated Feb 9, 2021: MR Conditional Sticky Pad Electrode.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 9, 2021 | MR Conditional Sticky Pad ElectrodeK203079 · GXY | 510(k) clearances |
| May 27, 2020 | Guardian Needle ElectrodeK200984 · GXZ | 510(k) clearances |
| Aug 5, 2019 | EEG Electrode TemplateK191225 · GXY | 510(k) clearances |
| Jul 10, 2019 | PressOn Electrode HeadsetK190801 · GXZ | 510(k) clearances |
| Dec 1, 2017 | MR Conditional Cup Electrode, MR Conditional Webb ElectrodeK172503 · GXY | 510(k) clearances |
| Apr 11, 2014 | RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBEK132138 · PDQ | 510(k) clearances |
| Jul 22, 2013 | MR CONDITIONAL PRESSON ELECTRODEK130220 · GXZ | 510(k) clearances |
| May 30, 2013 | MR CONDITIONAL CUP ELECTRODE, MR CONDITIONAL WEBB ELECTRODEK130287 · GXY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
