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 Advanced Medical Instruments with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 1, 1993: SYSTEM 7110 NON-INVASIVE BLOOD PRESSURE MONITOR.
| Jul 1, 1993 | SYSTEM 7110 NON-INVASIVE BLOOD PRESSURE MONITORK923595 · DXN | 510(k) clearances |
| May 13, 1993 | SYSTEM 7500 NIBP/SA02K924910 · DXN | 510(k) clearances |
| Apr 18, 1991 | SYSTEM 7300 PULSE OXIMETERK910521 · DQA | 510(k) clearances |
| Oct 23, 1990 | SYSTEM 7100 NON-INVASIVE BLOOD PRESSURE MONITORK897173 · DXN | 510(k) clearances |
| Jan 19, 1990 | DISP. NEONATAL BLOOD PRESSURE MONITORING CUFFK896788 · DXQ | 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
