510(k) Report

FDA applicant

V. Mueller O.V. Baxter Healthcare Corp.

Mchenry, IL41 decisions1976–19810 recalls

FDA records 41 decisions for V. Mueller O.V. Baxter Healthcare Corp. (Mchenry, IL) from 1976 to 1981: 41 510(k) clearances. Most are in product codes HNC (Specula, Ophthalmic) and FAJ (Cystoscope And Accessories, Flexible/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, gastroenterology and urology panel, where it files most

How often FDA has decided V. Mueller O.V. Baxter Healthcare Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for V. Mueller O.V. Baxter Healthcare Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — V. Mueller O.V. Baxter Healthcare Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like V. Mueller O.V. Baxter Healthcare Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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