510(k) Report

FDA applicant

Inhal-O-Tech Medical Plastic

Blue Springs, MO7 decisions1976–19780 recalls

FDA records 7 decisions for Inhal-O-Tech Medical Plastic (Blue Springs, MO) from 1976 to 1978: 7 510(k) clearances. Most are in product codes BYG (Mask, Oxygen) and KPD (Strip, Temperature, Forehead, Liquid Crystal). 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, anesthesiology panel, where it files most

How often FDA has decided Inhal-O-Tech Medical Plastic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inhal-O-Tech Medical Plastic since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inhal-O-Tech Medical Plastic by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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