FDA applicant

R. J. Doyle, Inc.

Spirit Lake, ID10 decisions1987–19890 recalls

FDA records 10 decisions for R. J. Doyle, Inc. (Spirit Lake, ID) from 1987 to 1989: 10 510(k) clearances. Most are in product codes BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)) and GAA (Needle, Aspiration And Injection, Disposable). 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 R. J. Doyle, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for R. J. Doyle, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — R. J. Doyle, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like R. J. Doyle, Inc.’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

R. J. Doyle, Inc.

Which product codes does it file in?

What has FDA decided for it lately?