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 13, 2026, FDA's public records list Electro-Catheter Corp. with 35 510(k) clearances. The most recent is a 510(k) clearance dated Jul 27, 1995: MULTIPACE.
| Jul 27, 1995 | MULTIPACEK934785 · LDF | 510(k) clearances |
| Apr 19, 1995 | OPEN TIP MULTI-ELECTRODE CATHETER, MODIFICATIONK933451 · DRF | 510(k) clearances |
| Apr 19, 1995 | CLOSED TIP MULTI-ELECTRODE CATHETER, MODIFICATIONK933450 · DRF | 510(k) clearances |
| Apr 19, 1995 | TIP DEFLECTOR (GENESIS)K943257 · DRF | 510(k) clearances |
| Feb 24, 1995 | SILICORE SEMI-FLOATERK934787 · LDF | 510(k) clearances |
| Apr 29, 1988 | ELECATH(R) TRANSESOPHAGEAL PACING CATHETERK874154 · KNT | 510(k) clearances |
| Feb 10, 1986 | ELECATH PERCUTANEOUS LEFT ATRIAL CANNULATION SETK854511 · DQX | 510(k) clearances |
| Jan 15, 1986 | ELECATH PULSATILE PERFUSION PUMPK854975 · KFM | 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
