510(k) Report

FDA applicant

Ets Rene Marzet

Mchenry, IL3 decisions1979–19800 recalls

FDA records 3 decisions for Ets Rene Marzet (Mchenry, IL) from 1979 to 1980: 3 510(k) clearances. Most are in product codes KNC (Table, Obstetric (And Accessories)) and FPO (Stretcher, Wheeled). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Ets Rene Marzet since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ets Rene Marzet’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