510(k) Report

FDA applicant

Alliance Instruments

Vancouver, WA1 decision1999–19990 recalls

FDA records 1 decision for Alliance Instruments (Vancouver, WA) in 1999: 1 510(k) clearance. All are in product code MWI (Monitor, Physiological, Patient (Without…). 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 Alliance Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alliance Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Alliance Instruments 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?

  • MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K980688Integriti Patient MonitorAlliance Instruments · 19992cite it

What has FDA decided for it lately?

  • K980688Integriti Patient MonitorAlliance Instruments · 1999

The one decision as Alliance Instruments →

Other applicant names beginning “Alliance”

FDA records each applicant name separately; these may or may not be the same firm.

Alliance Medical Corp. 47Alliance Rubber Products Sdn. Bhd. 12Alliance Partners, LLC 10Alliance Pharmaceutical Corp. 2Alliance International Co., Ltd. 2Alliance Global Technology Co., Ltd. 2Alliance Medical Technologies, Inc. 1Alliance Global 1Alliance Tech Medical, Inc. 1Alliance Medical Marketinig 1