510(k) Report

FDA applicant

Advanced Medical Instruments, Inc.

Broken Arrow, OK5 decisions1990–19930 recalls

FDA records 5 decisions for Advanced Medical Instruments, Inc. (Broken Arrow, OK) from 1990 to 1993: 5 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and DXQ (Blood Pressure Cuff). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Advanced Medical Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Medical Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DXNSystem, Measurement, Blood-Pressure, Non-Invasive3decisions
  • DXQBlood Pressure Cuff1decision
  • DQAOximeter1decision

What has FDA decided for it lately?

  • K923595System 7110 Non-Invasive Blood Pressure MonitorAdvanced Medical Instruments, Inc. · 1993
  • K924910System 7500 Nibp/SA02Advanced Medical Instruments, Inc. · 1993
  • K910521System 7300 Pulse OximeterAdvanced Medical Instruments, Inc. · 1991
  • K897173System 7100 Non-Invasive Blood Pressure MonitorAdvanced Medical Instruments, Inc. · 1990
  • K896788Disp. Neonatal Blood Pressure Monitoring CuffAdvanced Medical Instruments, Inc. · 1990

All 5 as Advanced Medical Instruments, Inc. →