510(k) Report

FDA applicant

Aquarius Medical Services

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Aquarius Medical Services (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code IOQ (Bed, Flotation Therapy, Powered). 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 Aquarius Medical Services’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aquarius Medical Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Aquarius”

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