FDA applicant

Bill Olson Corp.

Ocala, FL4 decisions1991–19980 recalls

FDA records 4 decisions for Bill Olson Corp. (Ocala, FL) from 1991 to 1998: 4 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and CAH (Filter, Bacterial, Breathing-Circuit). 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 Bill Olson Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bill Olson Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Bill”

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

Bill Dude Hospital Disposables, Inc. 1

Bill Olson Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bill”