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 North American Instrument Corp. with 28 510(k) clearances. The most recent is a 510(k) clearance dated Mar 29, 1996: SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS).
| Mar 29, 1996 | SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)K960801 · DQO | 510(k) clearances |
| Mar 4, 1996 | HEMO-VALVEK955554 · DTL | 510(k) clearances |
| Feb 7, 1996 | EPIC INTRODUCER SHEATHK960310 · DYB | 510(k) clearances |
| Mar 3, 1993 | MORSE(R) ANGIOGRAPHIC CATHETERSK922552 · DQO | 510(k) clearances |
| Jun 10, 1992 | MORSE HEMOSTATIC CATHETER INTRODUCER SETK915078 · DYB | 510(k) clearances |
| Jan 10, 1992 | MORSE ANESTHESIAK905208 · FPA | 510(k) clearances |
| Sep 11, 1991 | MORSE VASCULAR INTRODUCER SETK912961 · DYB | 510(k) clearances |
| Apr 22, 1991 | THE PERCEPTOR(TM) STAND ALONE TRANSDUCERK910764 · DRS | 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
