FDA applicant

Merivaara Instrumentarium Corp.

Washington, DC4 decisions1994–19940 recalls

FDA records 4 decisions for Merivaara Instrumentarium Corp. (Washington, DC) in 1994: 4 510(k) clearances. Most are in product codes FPO (Stretcher, Wheeled) and FNK (Bed, Hydraulic, Adjustable Hospital). 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, general hospital panel, where it files most

How often FDA has decided Merivaara Instrumentarium Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Merivaara Instrumentarium Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Merivaara Instrumentarium Corp.

Which product codes does it file in?

What has FDA decided for it lately?