510(k) Report

FDA applicant

Beta Medical Products Co.

Akron, OH3 decisions1986–19950 recalls

FDA records 3 decisions for Beta Medical Products Co. (Akron, OH) from 1986 to 1995: 3 510(k) clearances. Most are in product codes FPO (Stretcher, Wheeled) and IXR (Table, Radiographic, Tilting). No recall is linked to its devices.

FDA’s records also spell it “Beta Medical Products, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Beta Medical Products Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Beta Medical Products Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Beta Medical Products Co.’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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Other applicant names beginning “Beta”

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