FDA applicant

Loversan

Mchenry, IL3 decisions1984–19840 recalls

FDA records 3 decisions for Loversan (Mchenry, IL) in 1984: 3 510(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 Loversan’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Loversan since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Loversan

Which product codes does it file in?

What has FDA decided for it lately?