FDA applicant

Steven K. Juhn

Minneapolis, MN1 decision1986–19860 recalls

FDA records 1 decision for Steven K. Juhn (Minneapolis, MN) in 1986: 1 510(k) clearance. All are in product code JZF (Tube, Ear Suction). 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 Steven K. Juhn’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Steven K. Juhn since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Steven”

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

Steven H. Warnock, M.D. 1 Steven Frank Mercereau 1 Steven B. Lamberg, Dds 1 Steven K. Sue 1 Steven Chen 1 Steven Lamberg, D.D.S 1

Steven K. Juhn

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Steven”