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., part of AbbottLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list EP MedSystems with 15 510(k) clearances. The most recent is a 510(k) clearance dated Oct 16, 2009: EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04.
| Oct 16, 2009 | EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04K092913 · JOQ | 510(k) clearances |
| Mar 11, 2008 | MODIFICATION TO VIEWMATE SYSTEMK073709 · IYN | 510(k) clearances |
| May 1, 2007 | VIEWMATE SYSTEMK071028 · ITN | 510(k) clearances |
| Apr 11, 2007 | EP-WORKMATEK070706 · DQK | 510(k) clearances |
| Nov 30, 2006 | MAPMATEK063277 · DQK | 510(k) clearances |
| Oct 27, 2006 | EP-WORKMATEK063113 · DQK | 510(k) clearances |
| Sep 14, 2004 | EP-4 CLINICAL STIMUTATORK041442 · JOQ | 510(k) clearances |
| Apr 15, 2004 | EP DEFLECTABLE CATHETERSK033963 · DRF | 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
