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 Advance Medical Device, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 11, 1997: AMD HOME HEALTH MONITOR SYSTEM AND AMD MONITORING STATION.
| Feb 11, 1997 | AMD HOME HEALTH MONITOR SYSTEM AND AMD MONITORING STATIONK964697 · DXN | 510(k) clearances |
| Nov 21, 1995 | FLOSCOPE SUPER VASCULAR LABK943200 · JAF | 510(k) clearances |
| Mar 21, 1991 | FLOSCOPE MICRODOPK910441 · DPT | 510(k) clearances |
| Mar 15, 1991 | FLOSCOPE VASCULAR LAB.K905157 · JOP | 510(k) clearances |
| Sep 12, 1990 | PHYSICIAN'S CHOICEK903744 · HIB | 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
