510(k) Report

FDA applicant

Victor John Manley

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Victor John Manley (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code INW (Table, Mechanical). 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, physical medicine panel, where it files most

How often FDA has decided Victor John Manley’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Victor John Manley since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Victor John Manley’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 “Victor”

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