FDA applicant

Argosy Electronics

Eden Prairie, MN24 decisions1993–19980 recalls

FDA records 24 decisions for Argosy Electronics (Eden Prairie, MN) from 1993 to 1998: 24 510(k) clearances. All are in product code ESD (Hearing Aid, Air-Conduction, Prescription). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Argosy Electronics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Argosy”

FDA records each applicant name separately; these may or may not be the same firm.

Argosy Intl. (Usa), Inc. 14

Argosy Electronics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Argosy”