510(k) Report

FDA applicant

Perry Baromedical Services

Riviera Beach, FL4 decisions1986–19990 recalls

FDA records 4 decisions for Perry Baromedical Services (Riviera Beach, FL) from 1986 to 1999: 4 510(k) clearances. Most are in product codes CBF (Chamber, Hyperbaric) and CBK (Ventilator, Continuous, Facility Use). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Perry Baromedical Services’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Perry Baromedical Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Perry Baromedical 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 “Perry”

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