FDA applicant

Jufrey Multimed Corp.

Washington, DC7 decisions1985–19860 recalls

FDA records 7 decisions for Jufrey Multimed Corp. (Washington, DC) from 1985 to 1986: 7 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and BRZ (Set, Blood Transfusion). 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 Jufrey Multimed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jufrey Multimed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Jufrey Multimed Corp.

Which product codes does it file in?

What has FDA decided for it lately?