FDA applicant

Oxford Instruments Medical Systems

Clearwater, FL5 decisions1995–20010 recalls

FDA records 5 decisions for Oxford Instruments Medical Systems (Clearwater, FL) from 1995 to 2001: 5 510(k) clearances. Most are in product codes DSH (Recorder, Magnetic Tape, Medical) and HGM (System, Monitoring, Perinatal). Its devices cite 2 predicates, 1 of them its own earlier devices. 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 Oxford Instruments Medical Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oxford Instruments Medical Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Oxford Instruments Medical Systems’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Oxford”

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

Oxford Medilog, Inc. 48 Oxford Laboratories, Inc. 9 Oxford Instruments, Plc. 7 Oxford Performance Materials, Inc. 6 Oxford Biosignals Limited 4 Oxford Metrics, Inc. 2 Oxford Medical, Inc. 2 Oxford Instruments Medical, Ltd. 1 Oxford Brain Diagnostics, Ltd. 1 Oxford Immunotec, Ltd. 1

Oxford Instruments Medical Systems

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Oxford”