FDA applicant

Douglas Scientific Products

Mchenry, IL2 decisions1980–19820 recalls

FDA records 2 decisions for Douglas Scientific Products (Mchenry, IL) from 1980 to 1982: 2 510(k) clearances. Most are in product codes FLS (Monitor, Apnea, Facility Use) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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 Douglas Scientific Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Douglas Scientific Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Douglas”

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

Douglas Medical Products Corp. 20 Douglas James Donaldson Compliance Services 5 Douglas C. Yoon, Dds 1 Douglas Manufacturer Co. 1 Douglas Products 1 Douglas C. Mckee & Co. 1 Douglas Bueschel 1

Douglas Scientific Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Douglas”