510(k) Report

FDA applicant

Ohio Medical Products

Mchenry, IL47 decisions1976–19841 recall

FDA records 47 decisions for Ohio Medical Products (Mchenry, IL) from 1976 to 1984: 47 510(k) clearances. Most are in product codes BSZ (Gas-Machine, Anesthesia) and CBK (Ventilator, Continuous, Facility Use). 1 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, anesthesiology panel, where it files most

How often FDA has decided Ohio Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ohio Medical Products since 2007.

Recalls per year

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Ohio”

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