FDA applicant

Medical Emergency Support Equipment

St. Charles, MO1 decision1993–19930 recalls

FDA records 1 decision for Medical Emergency Support Equipment (St. Charles, MO) in 1993: 1 510(k) clearance. All are in product code IQK (Orthosis, Cervical). 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, physical medicine panel, where it files most

How often FDA has decided Medical Emergency Support Equipment’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Emergency Support Equipment since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Emergency Support Equipment

Which product codes does it file in?

What has FDA decided for it lately?