510(k) Report

FDA applicant

Michael S. Upsher

Mchenry, IL2 decisions1983–19830 recalls

FDA records 2 decisions for Michael S. Upsher (Mchenry, IL) in 1983: 2 510(k) clearances. All are in product code CCW (Laryngoscope, Rigid). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Michael S. Upsher since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Michael S. Upsher’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Michael”

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