Medical device makerLabelled 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 Intec Medical with 17 510(k) clearances. The most recent is a 510(k) clearance dated Jun 3, 1991: INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETER.
| Jun 3, 1991 | INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETERK911840 · DYG | 510(k) clearances |
| Oct 19, 1990 | THE GUIDER CORONARY GUIDING CATHETERK903216 · DQY | 510(k) clearances |
| Oct 19, 1990 | INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETERK900710 · KRB | 510(k) clearances |
| Oct 19, 1990 | TAPERED TIP THE GUIDER CORONARY GUIDING CATHETERK903217 · DQY | 510(k) clearances |
| Oct 16, 1990 | GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSYK903840 · DYB | 510(k) clearances |
| Sep 26, 1990 | PERCUTANEOUS CATHETER INTRODUCER KITK903906 · DYB | 510(k) clearances |
| Aug 14, 1990 | INTERVENTIONAL MEDICAL Y ADAPTER W/ADJUST. VALVEK900998 · DQY | 510(k) clearances |
| Jul 31, 1990 | TRI ADAPTER W/ADJUSTABLE HEMOSTASIS VALVESK901247 · DYG | 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
