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 13, 2026, FDA's public records list Intensive Technology, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jan 13, 1993: INTRA-OPERATIVE TEC ATHERECTOMY SYSTEM.
| Date | Record | Source |
|---|---|---|
| Jan 13, 1993 | INTRA-OPERATIVE TEC ATHERECTOMY SYSTEMK922970 · MCW | 510(k) clearances |
| Aug 24, 1992 | TEC ROTATING DUAL HEMOVALVEK912664 · DYB | 510(k) clearances |
| Oct 16, 1991 | IVT GUIDING CATHETERK911869 · DQY | 510(k) clearances |
| Jan 3, 1991 | IVT INTRODUCER SHEATHK903463 · DYB | 510(k) clearances |
| Nov 29, 1990 | HEMOCHRON(R) HEPARIN RESPONSE TESTK904003 · KFF | 510(k) clearances |
| Jun 28, 1990 | MODIFIED IVT PERIPHERAL ATHERECTOMYK901767 · LIT | 510(k) clearances |
| Mar 6, 1990 | MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEMK896403 · LIT | 510(k) clearances |
| Jan 4, 1990 | IVT 0.014 GUIDE WIREK895903 · DQX | 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
