FDA applicant

Hmba

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Hmba (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code DRI (Monitor, Line Isolation). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Hmba since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Hmba

Which product codes does it file in?

What has FDA decided for it lately?