510(k) Report

FDA applicant

Diagnostic Medical Instruments

Syracuse, NY5 decisions1983–19920 recalls

FDA records 5 decisions for Diagnostic Medical Instruments (Syracuse, NY) from 1983 to 1992: 5 510(k) clearances. Most are in product codes DSI (Detector And Alarm, Arrhythmia) and DSH (Recorder, Magnetic Tape, Medical). 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 Diagnostic Medical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diagnostic Medical Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Diagnostic”

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