FDA applicant

Oxford Medilog, Inc.

Clearwater, FL48 decisions1978–19940 recalls

FDA records 48 decisions for Oxford Medilog, Inc. (Clearwater, FL) from 1978 to 1994: 48 510(k) clearances. Most are in product codes DSI (Detector And Alarm, Arrhythmia) and GWQ (Full-Montage Standard Electroencephalograph). 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 Medilog, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oxford Medilog, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Laboratories, Inc. 9 Oxford Instruments, Plc. 7 Oxford Performance Materials, Inc. 6 Oxford Instruments Medical Systems 5 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 Medilog, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Oxford”